# FewerJobs export - 100 curated jobs Generated: 2026-08-12T01:42:25.422Z Source: https://fewerjobs.com ## Filters applied - **q**: Stoke Therapeutics - **quality_floor**: default - **match_401k_strict**: true - **parental_strict**: true - **non_birth_strict**: true - **pto_strict**: true - **include_older**: false - **apply_url_verified**: false - **page**: 1 - **per_page**: 100 - **sort**: relevance ## Jobs ### Director, Strategic Purchasing - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $173K-$221K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4677895006 - Excerpt: Director, Strategic Purchasing Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: We are seeking a Strategic Purchasing Director. In this newly created position, you will lead Stoke's strategic sourcing and procurement function as we continue to grow into a later stage clinical development and potentially commercial biotechnology company. Reporting to the VP, Controller, you will have the opportunity to establish this critical function and build it as the company grows. A key component of this role is to build and manage long-term, mutually beneficial vendor relationships that drive value and support the company's mission to address the underlying cause of severe diseases. Additionally, you will act as a strategic partner with functional business partners across the company, in particular clinical development, clinical ### Pharmacovigilance Scientist - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $237K-$270K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4678619006 - Excerpt: Pharmacovigilance Scientist Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: We are building our Pharmacovigilance department in support of ongoing clinical development activities and NDA submission for a first-in-class antisense oligonucleotide (ASO) therapy in a rare pediatric neurological disease. The PV Scientist is a newly created role and a genuine opportunity to shape the scientific infrastructure of PV department at a critical inflection point. The PV Scientist is accountable for overall PV science support for pharmacovigilance department at Stoke, which includes working in collaboration with the Safety Physician(s) and cross-functional teams to lead signal detection activities conducted in the safety governance model within the company. The ideal candidate will have deep PV science experience and will contribute across clinical and regulatory workstreams ### Senior Director, Clinical Quality Compliance - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $265K-$290K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4673473006 - Excerpt: Senior Director, Clinical Quality Compliance Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: The Sr. Director, Clinical Quality Compliance, will be responsible for overseeing all aspects of GCP and GCLP associated with the development, maintenance and oversight of activities related to Clinical Trials sponsored by Stoke. This role will report into The VP of Quality and will partner closely with other cross-functional groups such as Clinical Development, Clinical Development Operations, DMPK, Toxicology, Regulatory and other functions within Quality to embed GCP quality considerations into clinical development. This person will lead clinical quality strategy across Stoke's clinical programs. This role ensures global GCP and GCLP compliance (e.g., FDA, EMA, ICH etc.), provides guidance on clinical trial operations, and fosters a culture of quality, ### Associate Director, HCP Marketing - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $201K-$251K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4674243006 - Excerpt: Associate Director, HCP Marketing Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: The Associate Director, HCP Marketing will report to the Executive Director, Marketing. Along with the Executive Director of Marketing, you will be responsible for all HCP activities from disease education (DE) campaign development and deployment, as well as the creation of the branded campaign for the potential launch of zorevunersen. We are looking for someone with a particular expertise in non-personal marketing, but experience in others areas, such as KOL engagement, market research and congress strategy & execution, are a bonus. As a small company, we operate at a fast pace with many competing priorities so the ability to thrive in this type of requirement is essential. Key Responsibilities: Work ### Vice President, Field Leader, Market Access Field National & Regional - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $299K-$375K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4661908006 - Excerpt: Vice President, Field Leader, Market Access Field National & Regional Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: The Executive Director/Vice President, Field Leader - Market Access Field National & Regional will be responsible for building and leading Stoke's market access organization, including Market Access Account Directors (MADs) and Field Reimbursement Managers (FRMs). This leader will develop and execute the field strategy to ensure broad, timely, and sustained access to Zorevunersen across payers and ensure provider sites are compliantly supported on reimbursement processes. The role will focus on establishing trusted relationships with national and regional payers, Commercial and Medicaid, along with healthcare providers to minimize barriers to patient access. As part of the Market Access leadership team, this individual will play a ### Director, Financial Planning & Analysis (R&D) - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $214K-$243K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4677888006 - Excerpt: Director, Financial Planning & Analysis (R&D) Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: The Director, Financial Planning & Analysis (R&D) will play a critical role in financial and strategic decision making at the Company, playing a key role in the future growth of the organization. The focus of this position will be to provide overall financial business partnering to the Research & Development (R&D) functions including leading the budgeting, forecasting and long-range planning processes, supporting the monthly and quarterly close process, providing monthly reporting to department leads and the Executive Leadership Team, supporting external collaborations, and performing ad hoc financial analysis. This person will work closely with team members, department heads and program teams to understand and manage the performance of ### Sr. Medical Director, Pharmacovigilance - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $327K-$360K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4671447006 - Excerpt: Sr. Medical Director, Pharmacovigilance Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: The Senior Medical Director, Pharmacovigilance will be responsible for the medical review of adverse event data, the development of company causality assessment frameworks in post-marketing surveillance, and leading signal detection and management activities. This individual will work in close partnership with PV operations to build rigorous, scalable, medical safety practices suited to a clinical development and complex postmarketing environment. This position will report into the Head of Pharmacovigilance. This is a role for a physician who is energized by developing business practice frameworks and review processes that a growing medical safety function requires and leading the medical safety domain within the organization. Rare disease carries meaningful responsibility to patient and ### Director/Senior Director, Global Medical Information & Operations - Stoke Therapeutics - Location: Bedford, Massachusetts, United States (unspecified) - Salary: $232K-$321K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://www.stoketherapeutics.com/careers/job-opportunities/?gh_jid=4675891006 - Excerpt: Director/Senior Director, Global Medical Information & Operations Bedford, Massachusetts, United States About Stoke: Stoke Therapeutics (Nasdaq: STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body's potential with RNA medicine. Using Stoke's proprietary TANGO (Targeted Augmentation of Nuclear Gene Output) approach, Stoke is developing antisense oligonucleotides (ASOs) to selectively restore naturally-occurring protein levels. Stoke's first medicine in development, zorevunersen, has demonstrated the potential for disease modification in patients with Dravet syndrome and is currently being evaluated in a Phase 3 study. Stoke's initial focus are diseases of the central nervous system and the eye that are caused by a loss of ~50% of normal protein levels (haploinsufficiency). Proof of concept has been demonstrated in other organs, tissues, and systems, supporting broad potential for Stoke's proprietary approach. Stoke is headquartered in Bedford, Massachusetts. For more information, visit https://www.stoketherapeutics.com/ Position Purpose: Stoke Therapeutics is seeking an experienced and hands-on Medical Information leader to build, operationalize, and scale the Medical Information (MI) function in advance of commercialization. This role will have end-to-end ownership of Medical Information, including contact center strategy and operations, scientific response content, inquiry management, and development of a scalable, digitally enabled self-service medical information portal. This role requires strong operational rigor and a forward-looking mindset, with comfort working in ambiguity and establishing new ways of working. The ideal candidate brings a balance of scientific credibility, operational excellence, and curiosity about how Medical Information can continue to evolve in a growing organization. Key Responsibilities: Medical Information Strategy ### Band 5 - Chemotherapy Nurse - Stoke-on-Trent - Pulse Active Stations Network - Location: Stoke-on-Trent (unspecified) - Salary: Not disclosed - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/pulse/jobs/6512190003 - Excerpt: Band 5 - Chemotherapy Nurse - Stoke-on-Trent Stoke-on-Trent ### VodafoneThree - Incident Specialist - Vodafone Group - Location: Stoke on Trent, United Kingdom | ST1 5GP | Stoke-on-Trent ST1 5GP, UK (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://vodafone.eightfold.ai/careers/job/563018697039049 - Excerpt: VodafoneThree - Incident Specialist Stoke on Trent, United Kingdom | ST1 5GP | Stoke-on-Trent ST1 5GP, UK ### Short-term Temporary Team Member - Stoke Talke Outlet (N119972) - Next plc - Location: Stoke-On-Trent, Staffordshire, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://ekeq.fa.em2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_3001/requisitions/job/N119972 - Excerpt: Short-term Temporary Team Member - Stoke Talke Outlet (N119972) Stoke-On-Trent, Staffordshire, United Kingdom SHIFTS YOU ARE APPLYING FOR: 5.50hrs p/w; Sat 12:00 - 18:00 ### Short-term Temporary Team Member - Stoke Talke Outlet (N119971) - Next plc - Location: Stoke-On-Trent, Staffordshire, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://ekeq.fa.em2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_3001/requisitions/job/N119971 - Excerpt: Short-term Temporary Team Member - Stoke Talke Outlet (N119971) Stoke-On-Trent, Staffordshire, United Kingdom SHIFTS YOU ARE APPLYING FOR: 5.50hrs p/w; Sat 11:00 - 17:00 ### Short-term Temporary Team Member - Stoke Talke Outlet (N119973) - Next plc - Location: Stoke-On-Trent, Staffordshire, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://ekeq.fa.em2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_3001/requisitions/job/N119973 - Excerpt: Short-term Temporary Team Member - Stoke Talke Outlet (N119973) Stoke-On-Trent, Staffordshire, United Kingdom SHIFTS YOU ARE APPLYING FOR: 5.50hrs p/w; Sat 09:00 - 15:00 ### Short-term Temporary Team Member - Stoke Talke Outlet (N119974) - Next plc - Location: Stoke-On-Trent, Staffordshire, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://ekeq.fa.em2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_3001/requisitions/job/N119974 - Excerpt: Short-term Temporary Team Member - Stoke Talke Outlet (N119974) Stoke-On-Trent, Staffordshire, United Kingdom SHIFTS YOU ARE APPLYING FOR: 5.50hrs p/w; Sat 09:00 - 15:00 ### Short-term Temporary Team Member - Stoke Talke Outlet (N119970) - Next plc - Location: Stoke-On-Trent, Staffordshire, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://ekeq.fa.em2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_3001/requisitions/job/N119970 - Excerpt: Short-term Temporary Team Member - Stoke Talke Outlet (N119970) Stoke-On-Trent, Staffordshire, United Kingdom SHIFTS YOU ARE APPLYING FOR: 5.50hrs p/w; Sat 11:00 - 17:00 ### Therapeutic Area Head, Oncology - Bristol Myers Squibb - Location: Uxbridge - GB (unspecified) - Salary: Not disclosed - Posted: 2026-05-26 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Uxbridge---GB/Therapeutic-Area-Head--Oncology_R1602621 - Excerpt: Therapeutic Area Head, Oncology Uxbridge - GB posted: Posted 17 Days Ago ### Associate Director, Patient Services - Axsome Therapeutics - Location: New York, NY (unspecified) - Salary: $155K-$185K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5779343004 - Excerpt: Associate Director, Patient Services New York, NY Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role Axsome Therapeutics is seeking an Associate Director, Patient Services to lead the establishment and growth of a new Patient Services Hub. This role will work closely with the Director, Patient Services for developing, implementing, and overseeing all aspects of the Hub's operations, ensuring efficient and seamless patient access to therapies and support services. This role requires a strong leader to build and manage the hub team, foster collaborative relationships, and drive continuous improvement within a fast-paced environment. This role will have close collaboration among, and provide ad hoc support to, Field Access and Patient Service functions within the Market Access team, as related to the HUB. ### Industrial Engineer - Michelin - Location: Stoke On Trent (unspecified) - Salary: Not disclosed - Posted: 2026-05-21 - Apply: https://michelinhr.wd3.myworkdayjobs.com/Michelin/job/Stoke-On-Trent/Industrial-Engineer_R-2026020587 - Excerpt: Industrial Engineer Stoke On Trent posted: Posted 22 Days Ago ### Therapeutic Area Head, Psychiatry & Neuroscience Portfolio - Bristol Myers Squibb - Location: Uxbridge - GB (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Uxbridge---GB/Therapeutic-Area-Head--Psychiatry---Neuroscience-Portfolio_R1603331 - Excerpt: Therapeutic Area Head, Psychiatry & Neuroscience Portfolio Uxbridge - GB posted: Posted Yesterday ### Senior Medical Director, Oncology - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $298K-$351K - Posted: 2026-03-06 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5821320004 - Excerpt: Senior Medical Director, Oncology Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . Responsibilities: - Design and implement Phase I to III clinical studies - Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents - Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs - Act as a clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs - Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports - Act to provide medical oversight and safety monitoring for ongoing clinical trials including participation in SAE reporting and serving on the safety committee - Play a key role in the analysis, interpretation and delivery of high-quality clinical data - Interact with ### Senior Director, Regulatory Affairs - Netherlands - Corcept Therapeutics - Location: Amsterdam, North Holland, Netherlands (unspecified) - Salary: Not disclosed - Posted: 2026-03-20 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5799534004 - Excerpt: Senior Director, Regulatory Affairs - Netherlands Amsterdam, North Holland, Netherlands For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . As the Senior Director of Regulatory Affairs, you will architect and lead international regulatory strategy and execution to support Corcept's international commercialization and expansion, starting with Europe. This role ensures all regional and local regulatory requirements are met in cooperation with Corcept functions responsible for clinical research, manufacturing, and commercialization. Staying attuned to the evolving regulatory environment, you will assess and communicate the impact of changes on business and product development programs. At times, you will directly represent Corcept with health authorities in Europe and elsewhere, as our expansion continues. Responsibilities: - Develop robust European regulatory plans, aligned with Corcept's global strategy, that lead to commercialization in new countries - Provide regulatory guidance regarding European health authorities and interactions, including EMA - Contribute and independently execute the filing plans for Europe in line with corporate, regional, and ### HGV Driver Class 1 or Class 2 - Deutsche Post - Location: Stoke on Trent, Stoke On Trent, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-05-28 - 401(k) match: listed (not source-backed) - Apply: https://careers.uki.dsc.dhl/jobs/vacancy/hgv-driver-class-1-or-class-2-42280-stoke-on-trentvernon-road-stoke-on-trent/42301/description/action/apply?_channelid=30 - Excerpt: HGV Driver Class 1 or Class 2 Stoke on Trent, Stoke On Trent, United Kingdom LGV C+E or C Drivers (HGV 1 or 2) based Stoke on Trent. Pay Rate: £45,000 (OTE) including driver bonus, shift premiums & overtime. Contract Type: Permanent (Full-Time). Hours: Contracted to work 42... ### Associate Director/Director, Regulatory Affairs - Axsome Therapeutics - Location: New York, NY (unspecified) - Salary: $160K-$215K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5725020004 - Excerpt: Associate Director/Director, Regulatory Affairs New York, NY Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role Axsome Therapeutics is seeking an Associate Director/Director, Regulatory Affairs. The role is responsible for managing assigned regulatory activities for the development and commercialization of Axsome's product candidates. The right candidate will have had prior experience in independently providing regulatory guidance to investigational and commercial products under oversight provided by the department head when needed. The Associate Director/Director is responsible for mentoring associates as appropriate. This role reports directly to the VP, Regulatory Affairs. This role is based at Axsome's HQ in New York City with an on-site requirement of at least three days per week. We are unable to consider candidates who are looking for fully ### Senior Director/Vice President, Market Access - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $180K-$280K - Posted: 2026-04-21 - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8515744002 - Excerpt: Senior Director/Vice President, Market Access New York, NY Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As a Senior Director / Vice President of Market Access, you will be the backbone of the commercial organization. You will design the financial architecture of the product, shape the external policy and regulatory environments to support PDTs, and ensure long term viability of the PDT category. The role reports to the Chief Commercial Officer and ### Senior Director & Therapeutic Area Head, Regulatory Affairs - Revolution Medicines - Location: Redwood City, California, United States (unspecified) - Salary: $244K-$305K - Posted: 2026-04-10 - 401(k) match: listed (not source-backed) - Apply: https://www.revmed.com/careers-list/?gh_jid=7695273003 - Excerpt: Senior Director & Therapeutic Area Head, Regulatory Affairs Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: - Provide management and leadership of one or more therapeutic areas for late-stage oncology programs. - Oversee the development of global regulatory therapeutic area and product strategies to drive product development, global registration, , and effective regulatory agency interactions. - Provide regulatory expertise and guidance to therapeutic area commercialization teams and other governance bodies. - Foster the career development of staff within the therapeutic area and contribute to departmental leadership activities. - Ensure alignment and consistency across programs within a therapeutic area based on regulatory intel, research, and competitive landscape. Primary Responsibilities: - Direct the development of global regulatory strategy from registrational studies to marketing application across one or more therapeutic areas. - Lead and mentor GRLs/Study Leads in the development of global regulatory strategies, in partnership with regional regulatory leads, including precedence, risk management and contingency planning. - ### DBS Therapy Consultant - Atlanta, GA - Boston Scientific - Location: Atlanta, GA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.bostonscientific.com/job/Atlanta-DBS-Therapy-Consultant-Atlanta%2C-GA-GA-30301/1391017300/ - Excerpt: DBS Therapy Consultant - Atlanta, GA Atlanta, GA Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. Therapy Consultant for Deep Brain Stimulation Boston Scientific Neuromodulation About the role: At Boston Scientific Neuromodulation, you join a team that is focused on improving the lives of our patients through technology and service. Parkinson's Disease affects 10 million people worldwide, including more than 1 million in the US alone. Our global mission-our passion and purpose-is to support appropriate patients with cutting-edge technology. We are a global leader in Deep Brain Stimulation (DBS); and we launched that technology into the US market in 2018. If you have a passion for helping patients, a strategic mindset for advancing therapy in your local market, and the experience to support clinicians in complex cases; let's talk about how your skills paired with the Boston Scientific organization can advance Deep Brain Stimulation in your geography. Your responsibilities will include: Drive sales revenue to achieve territory objectives. Cultivating a customer base, continuously prospecting for new c ### Neuroscience Sales Specialist, Lafayette, LA - Acadia Pharmaceuticals Inc - Location: Louisiana - Remote (remote) - Salary: $92K-$115K - Posted: 2026-05-22 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://acadia.com/en-us/careers/job-board/8561966002?gh_jid=8561966002 - Excerpt: Neuroscience Sales Specialist, Lafayette, LA Louisiana - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Lafayette, LA Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare stakeholders. - Address customer questions, concerns, and objections using advanced dialogue and selling skills. - Tailor ### Neuroscience Sales Specialist - Allentown, PA - Acadia Pharmaceuticals Inc - Location: Pennsylvania - Remote (remote) - Salary: $92K-$115K - Posted: 2026-06-09 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://acadia.com/en-us/careers/job-board/8583072002?gh_jid=8583072002 - Excerpt: Neuroscience Sales Specialist - Allentown, PA Pennsylvania - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Allentown, PA Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare stakeholders. - Address customer questions, concerns, and objections using advanced dialogue and selling skills. - ### Neurovascular Product Marketing Manager for UK, Benelux & Nordics (m/f/d) - based in the UK - Penumbra, Inc. - Location: United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-04-02 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Apply: https://jobs.lever.co/penumbrainc/1b8ef4d1-b483-4c80-a411-694c0ae7059e - Excerpt: Neurovascular Product Marketing Manager for UK, Benelux & Nordics (m/f/d) - based in the UK United Kingdom At Penumbra,innovation,teamwork, andinitiativeare more than values - they are the foundation of a workplace where every individual is encouraged to grow and make a real difference. We believe that the strength of our team lies in our diverse talents and shared passion for improving lives. If you're looking for a role where your contributions matter, we invite you to join a company that values both personal development and impactful work. As a leading MedTech company, we provide cutting-edge solutions for conditions such as stroke, pulmonary embolism, deep vein thrombosis, and acute limb ischemia. Headquartered in Alameda, California, Penumbra has over 4,500 employees worldwide and generated revenues of approximately $1.4 billion in 2025. At Penumbra,innovation,teamwork, andinitiativeare more than values - they are the foundation of a workplace where every individual is encouraged to grow and make a real difference. We believe that the strength of our team lies in our diverse talents and shared passion for improving lives. If you're looking for a role where your contributions matter, we invite you to join a company that values both personal development and impactful work. As a leading MedTech company, we provide cutting-edge solutions for conditions such as stroke, pulmonary embolism, deep vein thrombosis, and acute limb ischemia. Headquartered in Alameda, California, Penumbra has over 4,500 employees worldwide and generated revenues of approximately $1.4 billion in 2025. What is in it for you - Stay Active ### Neurovascular Territory Manager London (m/f/d) - London - Penumbra, Inc. - Location: London (unspecified) - Salary: Not disclosed - Posted: 2026-04-28 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Apply: https://jobs.lever.co/penumbrainc/1f2600b9-ef55-4962-b0e6-815463924aec - Excerpt: Neurovascular Territory Manager London (m/f/d) - London London At Penumbra,innovation,teamwork, andinitiativeare more than values-they are the foundation of a workplace where every individual is encouraged to grow and make a real difference. We believe that the strength of our team lies in our diverse talents and shared passion for improving lives. Ifyou'relooking for a role where your contributions matter, we invite you to join a company that values both personal development and impactful work. As a leading MedTech company,weprovidecutting-edgesolutions for conditions such as stroke, pulmonary embolism, deep vein thrombosis, and acute limb ischemia.Headquarteredin Alameda, California, Penumbra has over 4,500 employees worldwide and generated revenues of approximately$1.4 billionin 2025. At Penumbra,innovation,teamwork, andinitiativeare more than values-they are the foundation of a workplace where every individual is encouraged to grow and make a real difference. We believe that the strength of our team lies in our diverse talents and shared passion for improving lives. Ifyou'relooking for a role where your contributions matter, we invite you to join a company that values both personal development and impactful work. As a leading MedTech company,weprovidecutting-edgesolutions for conditions such as stroke, pulmonary embolism, deep vein thrombosis, and acute limb ischemia.Headquarteredin Alameda, California, Penumbra has over 4,500 employees worldwide and generated revenues of approximately$1.4 billionin 2025. What is in it for you - Stay Active - Enjoy an annual fitness subsidy to support your healthy lifestyle. - Support & Well-Being - Benefit from our comprehensive Employee Assistance Program, providing guidance and support in times of need. - Family ### Technical Writer - Varex Imaging Corp - Location: Stoke on Trent (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://vareximaging.wd103.myworkdayjobs.com/External_Career_Site/job/Stoke-on-Trent/Technical-Writer_R0005799 - Excerpt: Technical Writer Stoke on Trent posted: Posted 30+ Days Ago ### Senior Director, Medical Affairs, UK - Revolution Medicines - Location: London, England, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-04-28 - 401(k) match: listed (not source-backed) - Apply: https://www.revmed.com/careers-list/?gh_jid=7717896003 - Excerpt: Senior Director, Medical Affairs, UK London, England, United Kingdom Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: Reporting to the VP, General Manager, UK the Senior Director, Medical Affairs, UK is the medical leader responsible for defining and executing the local medical strategy for oncology products. This role serves as the medical voice within the UK Leadership Team, ensuring scientific excellence, compliant medical engagement, and strong alignment between global strategy and local patient, physician, and healthcare system needs. This leader will ensure that UK medical considerations are embedded in the regional medical strategy and plans and will partner with the General Manager and crossfunctional teams, as well as the VP, Head of Europe Medical Affairs and their leadership team. The incumbent will contribute to building the UK medical team and work closely with the Global and Regional Medical Affairs teams across Med Affairs functions. Responsibilities: - Act as the Medical Affairs lead for UK, accountable for local medical strategy, execution, ### Clinical Sales Specialist (CS) - Flint, MI - Corcept Therapeutics - Location: Flint, Michigan, United States (unspecified) - Salary: $140K-$155K - Posted: 2026-05-28 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6008345004 - Excerpt: Clinical Sales Specialist (CS) - Flint, MI Flint, Michigan, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The CS is accountable for implementing the sales strategies for approved products consistent with Corcept's compliance standards as well as all applicable legal requirements for those key targeted health care providers and hospital systems within an assigned territory. Responsibilities: - Build and develop professional relationships with influential high prescribers and thought leaders in the territory to enhance Corcept brand and product loyalty - Leverages expertise and knowledge of the therapeutic disease state, the marketplace, applicable competitors, industry, and cross-functional activities/plans to anticipate and effectively manage business opportunities and challenges - Develops and implements effective customer specific territory plans and communicates insights to internal stakeholders - Prioritizes time and effort to ensure optimal coverage of appropriate physician specialists based on opportunity and potential - Plan and participate in education programs and speaker dinner programs - Manage territory ### Occupational Hygiene & SHE Technician - Michelin - Location: Stoke On Trent (unspecified) - Salary: Not disclosed - Posted: 2026-05-19 - Apply: https://michelinhr.wd3.myworkdayjobs.com/Michelin/job/Stoke-On-Trent/Site-Industrial-Hygiene---SHE-Technician_R-2026006918 - Excerpt: Occupational Hygiene & SHE Technician Stoke On Trent posted: Posted 24 Days Ago ### Project Manager - Varex Imaging Corp - Location: Stoke on Trent (unspecified) - Salary: Not disclosed - Posted: 2026-05-28 - 401(k) match: listed (not source-backed) - Apply: https://vareximaging.wd103.myworkdayjobs.com/External_Career_Site/job/Stoke-on-Trent/Project-Manager_R0005679 - Excerpt: Project Manager Stoke on Trent posted: Posted 15 Days Ago ### VodafoneThree - Channel Readiness Specialist - Vodafone Group - Location: Stoke on Trent, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://vodafone.eightfold.ai/careers/job/563018696221593 - Excerpt: VodafoneThree - Channel Readiness Specialist Stoke on Trent, United Kingdom ### Expression of Interest - AbbVie - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012586396-expression-of-interest-abbvie - Excerpt: Expression of Interest - AbbVie Westport, MO, Ireland Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description: Expression of Interest for AbbVie in Ireland At AbbVie, we are dedicated to improving lives through transformative medicines and innovative healthcare solutions. We are a global biopharmaceutical company that researches, develops, and manufactures advanced medicines that uplift and enhance patients' well-being. Every day at AbbVie counts - we harness passion and dedication to make a positive impact on health worldwide. When you join AbbVie, you can be assured that your efforts will contribute to the betterment of human health across the globe. With a substantial presence in Ireland, including sites in Cork, Dublin, Sligo, and Mayo, AbbVie is a key employer in the region. Our business thrives thanks to exceptional individuals with high-level technical capability and expertise. We excel in pioneering science, advancing research, and driving impactful healthcare innovations. Working at AbbVie As our business evolves through cutting-edge research, we are always eager to engage with talented individuals ready to join us on our mission. Interested in joining us on ### VodafoneThree - Complex Complaints Specialist - Vodafone Group - Location: Stoke on Trent, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://vodafone.eightfold.ai/careers/job/563018697073916 - Excerpt: VodafoneThree - Complex Complaints Specialist Stoke on Trent, United Kingdom ### Vice President, Drug Safety & Pharmacovigilance - Braveheart - Location: San Francisco, CA or Remote or Hybrid (hybrid) - Salary: $330K-$400K - Posted: 2026-05-20 - Apply: https://job-boards.greenhouse.io/braveheartbio/jobs/4254374009 - Excerpt: Vice President, Drug Safety & Pharmacovigilance San Francisco, CA or Remote or Hybrid About us: Braveheart Bio is a Bay Area-based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. Our lead program is a next-generation myosin inhibitor, licensed from Hengrui Pharma, being developed to transform the treatment of hypertrophic cardiomyopathy (HCM)-the most common inherited cardiac disease. Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our candidate has demonstrated a compelling clinical profile that may position it as a best-in-class therapy with meaningful differentiation. With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a high-profile and rapidly evolving therapeutic area. The role: The Vice President, Drug Safety and Pharmacovigilance will lead and scale the global drug safety and pharmacovigilance function at Braveheart Bio. Reporting into the Chief Medical Officer, the VP is accountable for the safety strategy and integrated benefit-risk profile across the portfolio, with immediate focus on supporting Phase 3 programs and preparing the organization for NDA submission and post-marketing readiness. The VP will partner with an established Senior Director of PV (a direct report) to design the PV operating model, select CRO/PV vendor partners, establish the safety governance framework, and represent Safety in cross-functional and regulatory interactions. This individual will be hands-on while setting strategic direction and has a track record of leveraging external partners to deliver inspection-ready DSPV at ### Systems Test Engineer - Varex Imaging Corp - Location: Stoke on Trent (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://vareximaging.wd103.myworkdayjobs.com/External_Career_Site/job/Stoke-on-Trent/Systems-Test-Engineer_R0005767 - Excerpt: Systems Test Engineer Stoke on Trent posted: Posted 30+ Days Ago ### Senior Director/VP, Medical Affairs - Click Therapeutics - Location: New York, NY, Boston, MA or Remote (remote) - Salary: $180K-$280K - Posted: 2026-04-29 - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8525471002 - Excerpt: Senior Director/VP, Medical Affairs New York, NY, Boston, MA or Remote Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As the Senior Director / Vice President of Medical Affairs, you will be the scientific heartbeat of the organization. You will act as the scientific authority for CT-155. This team generates the evidence (RWE/OLE) needed to prove clinical value and economic impact, supplying the "raw material" that Marketing and Access teams leverage. The ### VodafoneThree - Consumer Sales Adviser - Vodafone Group - Location: Stoke on Trent, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://vodafone.eightfold.ai/careers/job/563018696282480 - Excerpt: VodafoneThree - Consumer Sales Adviser Stoke on Trent, United Kingdom ### Neuroscience Sales Specialist - Southern New Jersey, NJ - Acadia Pharmaceuticals Inc - Location: New Jersey - Remote (remote) - Salary: $92K-$115K - Posted: 2026-05-19 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://acadia.com/en-us/careers/job-board/8554820002?gh_jid=8554820002 - Excerpt: Neuroscience Sales Specialist - Southern New Jersey, NJ New Jersey - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: Philadelphia, NJ Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare stakeholders. - Address customer questions, concerns, and objections using advanced dialogue and ### VodafoneThree - Customer Success Advisor - Vodafone Group - Location: Stoke on Trent, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://vodafone.eightfold.ai/careers/job/563018696897972 - Excerpt: VodafoneThree - Customer Success Advisor Stoke on Trent, United Kingdom ### Director, Product and Pipeline Communications (Endocrinology and Metabolic) - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $239K-$281K - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6019134004 - Excerpt: Director, Product and Pipeline Communications (Endocrinology and Metabolic) Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director of Product and Pipeline Communications will drive product communications initiatives and activities across a growing roster of therapeutic areas for our Endocrinology business and metabolic disease program. Reporting to the Senior Director of Corporate Communications, the Director of Product and Pipeline Communications will drive initiatives that support increased product awareness and bolster Corcept's corporate reputation, developing approaches to communication that improve engagement with external stakeholders and meet the evolving business needs of the organization. Responsibilities: - Partner with leaders throughout the organization to plan and execute strategic communications activities to raise visibility of our products and pipeline - Develop and implement communications plans leveraging earned media, sponsored content, social media and owned media channels to engage and inform media, investors, employees, healthcare professionals, consumers, policymakers, advocacy partners and other external stakeholders - ### VodafoneThree - Business Development Specialist, MNC - Vodafone Group - Location: Stoke on Trent, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://vodafone.eightfold.ai/careers/job/563018696323708 - Excerpt: VodafoneThree - Business Development Specialist, MNC Stoke on Trent, United Kingdom ### VodafoneThree - Account Manager, Multinational Customers - Vodafone Group - Location: Stoke on Trent, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://vodafone.eightfold.ai/careers/job/563018696815370 - Excerpt: VodafoneThree - Account Manager, Multinational Customers Stoke on Trent, United Kingdom ### DBS Therapy Consultant - Charlotte, NC - Boston Scientific - Location: Charlotte, NC (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.bostonscientific.com/job/Charlotte-DBS-Therapy-Consultant-Charlotte%2C-NC-NC-28201/1379687100/ - Excerpt: DBS Therapy Consultant - Charlotte, NC Charlotte, NC Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. Therapy Consultant for Deep Brain Stimulation Boston Scientific Neuromodulation About the role: At Boston Scientific Neuromodulation, you join a team that is focused on improving the lives of our patients through technology and service. Parkinson's Disease affects 10 million people worldwide, including more than 1 million in the US alone. Our global mission-our passion and purpose-is to support appropriate patients with cutting-edge technology. We are a global leader in Deep Brain Stimulation (DBS); and we launched that technology into the US market in 2018. If you have a passion for helping patients, a strategic mindset for advancing therapy in your local market, and the experience to support clinicians in complex cases; let's talk about how your skills paired with the Boston Scientific organization can advance Deep Brain Stimulation in your geography. Your responsibilities will include: Drive sales revenue to achieve territory objectives. Cultivating a customer base, continuously prospecting for new c ### Director, Pharmacovigilance Operations and Engagement - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $240K-$280K - Posted: 2026-02-04 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5790809004 - Excerpt: Director, Pharmacovigilance Operations and Engagement Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . This will serve as the PSPV lead for cross-functional activities and commercial initiatives, ensuring successful product launch and lifecycle management with patient safety integrated throughout the organization. This highly visible role will act as a strategic partner to Medical Affairs, Quality, Legal, and Commercial teams, driving operational and compliance excellence across all touchpoints. This is a hybrid role typically requiring on-site presence at least 3 days per week at company headquarters in Redwood City. Responsibilities: Cross-Functional Leadership & Collaboration: - Build strategic partnerships and alignment of patient safety objectives and deliverables with internal stakeholders (Medical Affairs, Quality, Legal, Commercial) and external vendors/partners - Establish and lead cross functional governance forum with PSPV, Medical Affairs, Quality, Legal, Commercial to review all commercial initiatives/activities for cross functional planning and execution - Act as the Safety Lead for implementation and ### Band 5 - Intensive Therapy Unit Nurse - Stoke-on-Trent - Pulse Active Stations Network - Location: Manchester (unspecified) - Salary: Not disclosed - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/pulse/jobs/7636857003 - Excerpt: Band 5 - Intensive Therapy Unit Nurse - Stoke-on-Trent Manchester ### Beauty Advisor - Estee Lauder - M&S Wolstanton - Estée Lauder Companies (The) - Location: Wolstanton Stoke,GB-STE,United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://elcompanies.eightfold.ai/careers/job/1168273185038 - Excerpt: Beauty Advisor - Estee Lauder - M&S Wolstanton Wolstanton Stoke,GB-STE,United Kingdom ### Senior Therapeutic Area Specialist, Neuroscience - Cobenfy - Allentown, PA - Bristol Myers Squibb - Location: Allentown - PA - US (unspecified) - Salary: Not disclosed - Posted: 2026-06-09 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Allentown---PA---US/Senior-Therapeutic-Area-Specialist--Neuroscience---Cobenfy---Allentown--PA_R1603369 - Excerpt: Senior Therapeutic Area Specialist, Neuroscience - Cobenfy - Allentown, PA Allentown - PA - US posted: Posted 3 Days Ago ### Associate Director, Regulatory Affairs - Tonix Pharmaceuticals Holding Corp - Location: Berkeley Heights, NJ or Frederick, MD or North Dartmouth, MA or Fort Worth, TX (unspecified) - Salary: $190K-$200K - Posted: 2026-04-14 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4215536009 - Excerpt: Associate Director, Regulatory Affairs Berkeley Heights, NJ or Frederick, MD or North Dartmouth, MA or Fort Worth, TX Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property ### Payroll & Benefits Specialist - Fixed term contract (12-18 months) - Michelin - Location: Stoke-On-Trent (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - Apply: https://michelinhr.wd3.myworkdayjobs.com/Michelin/job/Stoke-On-Trent/Payroll---Benefits-Specialist_R-2026022335 - Excerpt: Payroll & Benefits Specialist - Fixed term contract (12-18 months) Stoke-On-Trent posted: Posted 4 Days Ago ### Clinical Implementation Specialist - Midlands (Leicestershire/BSOL/ Derby and Derbyshire/Staffs and Stoke-on-trent) - DexCom - Location: Remote - United Kingdom (remote) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://dexcom.wd1.myworkdayjobs.com/Dexcom/job/Remote---United-Kingdom/Clinical-Implementation-Specialist---Midlands_JR117317-1 - Excerpt: Clinical Implementation Specialist - Midlands (Leicestershire/BSOL/ Derby and Derbyshire/Staffs and Stoke-on-trent) Remote - United Kingdom posted: Posted 30+ Days Ago ### Director, Market Access - DACH - Corcept Therapeutics - Location: Berlin, Berlin, Germany (unspecified) - Salary: Not disclosed - Posted: 2026-04-10 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5920705004 - Excerpt: Director, Market Access - DACH Berlin, Berlin, Germany For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director, Market Access is responsible for defining and executing the market access, pricing, and reimbursement strategy for Corcept's oncology portfolio in DACH. This role is critical to ensuring timely, sustainable, and compliant patient access through successful navigation of DACH complex access environment, including AMNOG, Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG) Bundesausschuss (G ‑ BA), Statutory Health Insurance (SHI) negotiations, and regional access dynamics. The Director will report to DACH GM and serve as the market access lead for DACH, partnering closely with U.S. Headquarters Market Access, Health Economics and Outcomes Research (HEOR), Medical, Commercial and Legal and Compliance to drive optimal launch readiness, reimbursement outcomes, and long ‑ term access success. Responsibilities: Market Access Strategy & Leadership - Develop and lead the DACH German market access strategy for Corcept's oncology assets across the product lifecycle, from ### Manager, Quality Assurance Operations - Netherlands - Corcept Therapeutics - Location: Amsterdam, North Holland, Netherlands (unspecified) - Salary: Not disclosed - Posted: 2026-03-20 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5829946004 - Excerpt: Manager, Quality Assurance Operations - Netherlands Amsterdam, North Holland, Netherlands For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Quality Assurance Operations Manager is responsible for a variety of operational activities pertaining to assuring product quality and compliance with the manufacture, testing, control, validation, and release of pharmaceutical drug substance and drug product for commercial and clinical distribution. This role will also be responsible for the oversight of 3PLs and work closely with the QPs to distribute products in EU. This is a remote role. Responsibilities: - Act as Quality lead and support in various Chemistry, Manufacturing and Controls (CMC) projects - Work cross-functionally with the CMC group to provide oversight and resolve quality investigations of issues that occur at contract manufacturing and testing organizations - Perform review of executed batch records and test data and perform product disposition - Review and approval of validation protocols and reports (e.g., process, method, etc.) - Lead and ### Site Maintenance Operative - Associated British Foods - Location: Stoke (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://careers.abfgrocery.com/AlliedBakeries/job/Stoke-Site-Maintenance-Operative-ST5-9HT/3917-en_GB/ - Excerpt: Site Maintenance Operative Stoke Overview of role 📍 Location: Stoke, Newcastle-under-Lyme 🕙 Hours: 42 per week, Monday-Friday 06:00 -14:30 with occasional weekends. 💰 Salary: From £30,000 Join Our Team! We currently have a fantastic opportunity for a site maintenance operative to join our team at Allied Bakeries, Stoke. The successful candidate will be responsible for supporting the site with all facilities and building requirements. The role liaises with a number of stakeholders across the business including employees at Stoke and Liverpool, suppliers and contractors. The working pattern is Monday to Friday with an occasional 1 day at weekends : 06:00 - 14:30, 42 hours per week. A degree of flexibility is required to meet our site needs and overtime will be paid as and when required. Key Accountabilities 🔹Safety always comes first at Allied Bakeries, so we are looking for someone to lead by example in ensuring that Health and Safety is our number one priority 🔹Carry out general site repairs and maintenance, including doors, floors, walls, ceilings, and fixtures 🔹Maintain site services such as lighting, basic plumbing, drainage, and utilities (excluding production machinery) 🔹Complete reactive repairs in response to reported issues across the site 🔹Support planned maintenance tasks to prevent damage or deterioration of the building 🔹Ensure work areas meet food safety, hygiene, and health & safety standards 🔹Carry out basic external maintenance, including walkways, and fencing 🔹Log completed work and report a ### Executive Director, Regulatory Affairs Advertising & Promotion - DYNE Therapeutics - Location: Waltham MA or Remote (remote) - Salary: $250K-$310K - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/dynetherapeutics/jobs/5743751004 - Excerpt: Executive Director, Regulatory Affairs Advertising & Promotion Waltham MA or Remote Company Overview: Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at https://www.dyne-tx.com/ , and follow us on X , LinkedIn and Facebook . Role Summary: The Executive Director, Regulatory Affairs Advertising & Promotion leads regulatory strategy and compliance for advertising and promotional activities across all external communications. This role serves as the subject matter expert, partnering with the launch team, commercial, medical affairs, R&D, corporate communications, legal, and leadership to ensure messaging aligns with FDA regulations and company objectives. The person in this role provides strategic guidance on complex promotional claims, anticipates market and regulatory factors, and drives innovative, compliant solutions. This role chairs the regulatory review for the Promotion Review Committee (PRC) and for the Medical Review Committee (MRC), balancing legal requirements with business goals while mitigating risk across promotional campaigns and corporate communications. This role can be located in Waltham or remotely with travel to our office per business needs. Primary Responsibilities Include : Serves as the s ubject matter ### Senior Field Test Engineer - Otis Worldwide - Location: Otis Bristol, Unit 2, Blenhiem Court, 6 Beaufort Park, Woodlands, Bradley Stoke Bristol, BS32 4NE, UK. (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://otis.wd5.myworkdayjobs.com/REC_Ext_Gateway/job/Otis-Bristol-Unit-2-Blenhiem-Court-6-Beaufort-Park-Woodlands-Bradley-Stoke-Bristol-BS32-4NE-UK/Senior-Field-Test-Engineer_20141809 - Excerpt: Senior Field Test Engineer Otis Bristol, Unit 2, Blenhiem Court, 6 Beaufort Park, Woodlands, Bradley Stoke Bristol, BS32 4NE, UK. posted: Posted 30+ Days Ago ### Senior Therapeutic Area Specialist, Neuroscience - Cobenfy; Birmingham, AL - Bristol Myers Squibb - Location: Birmingham - AL - US (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Birmingham---AL---US/Senior-Therapeutic-Area-Specialist--Neuroscience---Cobenfy--Birmingham--AL_R1599301 - Excerpt: Senior Therapeutic Area Specialist, Neuroscience - Cobenfy; Birmingham, AL Birmingham - AL - US posted: Posted 8 Days Ago ### Field Service Engineer - Stoke-on-Trent to Wrexham - Roche Holding AG - Location: London, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - Apply: https://roche.wd3.myworkdayjobs.com/roche-ext/job/United-Kingdom/Field-Service-Engineer---Stoke-on-Trent-to-Wrexham_202605-112263/apply - Excerpt: Field Service Engineer - Stoke-on-Trent to Wrexham London, United Kingdom Embrace the opportunity to become a Field Service Engineer and play a vital role in supporting innovative medical diagnostics across the UK. Leverage your technical expertise to troubleshoot, maintain, and deliver exceptional service to healthcare customers. Enjoy a dynamic, collaborative environment with opportunities for growth and impact in the IVD industry. ### Director, Clinical Quality Assurance - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $229K-$260K - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5995887004 - Excerpt: Director, Clinical Quality Assurance Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept. This is a hybrid role typically requiring on-site presence at least 3 days per week. Responsibilities: - Lead Clinical Quality Assurance activities as line manager to assigned CQA Leads and working with therapeutic area teams to support success of the clinical studies sponsored or supported by Corcept - Champion and influence management and growth of the Clinical Quality Assurance team with the goal of attracting and developing talent, creating a rewarding professional environment, and ensuring that the team's capabilities meet Corcept's future needs - Lead, manage, and train others on GCP audits, including clinical investigative site audits, clinical ### Customer Delivery Driver Class 2 - Associated British Foods - Location: Stoke (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://careers.abfgrocery.com/AlliedBakeries/job/Stoke-Customer-Delivery-Driver-Class-2-ST5-9HT/3756-en_GB/ - Excerpt: Customer Delivery Driver Class 2 Stoke Overview of role 📍 Location: Based in Stoke (Newcastle-under-Lyme) 🕙 Hours: 48 hours a week (5 days including a Saturday, 2am starts) 💰 Salary: £37,956.37 Join Our Team! Are you a skilled driver with a passion for excellence and safety? We're on the lookout for a qualified, experienced Class 2 Delivery Driver to join our expert team at our Stoke site. If you're ready to take on a role that values your dedication and expertise, this is the opportunity for you! Key Accountabilities 🔹Comply with all legal requirements for HGV Drivers. 🔹Deliver and collect products from customers, suppliers and other organisations and locations, as required by the business. 🔹To always drive Company vehicles to high standards of safety and courtesy, including compliance with the Highway Code and any Company standards 🔹To apply SAFED driving techniques, in order to maximise levels of safety and fuel efficiency. 🔹To comply with all Company delivery and collection procedures, e.g. picking from bulk order load, order adjustment, health and safety. 🔹To comply with Company standards for customer service. 🔹To report immediately to the FLM any variations to required standards of product quality and service levels 🔹To follow Company standards and procedures for working with, and accounting for, Company products and equipment, e.g. bread baskets, pallets, store returns and buffer stock. 🔹To comply with all Company requirements for Driver training and communications 🔹To carry out any duties, as required by t ### Neuroscience Sales Specialist - San Jose, CA - Acadia Pharmaceuticals Inc - Location: California - Remote (remote) - Salary: $124K-$155K - Posted: 2025-12-15 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://acadia.com/en-us/careers/job-board/8339288002?gh_jid=8339288002 - Excerpt: Neuroscience Sales Specialist - San Jose, CA California - Remote About Acadia Pharmaceuticals Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinson's disease psychosis and Rett syndrome. We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs. At Acadia, we're here to be their difference. Seeking talent near: San Jose, CA; Palo Alto, CA; Redwood Ctiy, CA; Santa Cruz, CA; Salinas, CA; Marina, CA Position Summary The Neuroscience Sales Specialist is responsible for achieving sales goals within the assigned territory by building strong customer relationships, delivering compliant and compelling product education, and driving appropriate patient access. This role requires expertise in neuroscience, deep knowledge of the local healthcare landscape, and the ability to partner effectively with healthcare professionals (HCPs) and key stakeholders to deliver meaningful value and service. Primary Responsibilities - Promote Acadia products to HCPs in person and virtually, providing clinical, disease state, and reimbursement information in a compliant and customer-focused manner. - Develop and execute a territory business plan to meet or exceed sales objectives, leveraging market data, customer insights, and quarterly action plans. - Establish and maintain strong relationships with HCPs, including key opinion leaders, advocacy organizations, and other healthcare ### Engineering Team Leader - Associated British Foods - Location: Stoke (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://careers.abfgrocery.com/AlliedBakeries/job/Stoke-Engineering-Team-Leader-ST5-9HT/3904-en_GB/ - Excerpt: Engineering Team Leader Stoke 📍 Location: Stoke (Newcastle-under-Lyme), Midlands 🕙 Hours: 4 on 4 off, 2 days 2 nights (12 hour shifts) 💰 Salary: £56,368.11 We have an exciting opportunity for a hands‑on Engineering Team Leader to join our bakery in Stoke. In this role, you'll lead your shift team on the front line, driving both proactive and reactive maintenance across our plant and site services. You'll play a key part in keeping a major bakery operation running smoothly, safely, and efficiently. What You'll Be Doing Safety is always first at Allied Bakeries, so we are looking for someone to lead by example in ensuring that Health and Safety is our number one priority, and someone who can engage others to always think and behave safely. 🔹Focusing on safe working practices and site performance KPI's including OEE and CCOs. 🔹Diagnosing and correcting automation, electrical and mechanical issues to resolve breakdown situations. 🔹Ensuring our engineering strategy is delivered consistently. 🔹Delivering turn-key improvement projects in a timely and cost-efficient manner. 🔹Driving the performance of the Engineering function forward through effective team leadership on shift, setting the standards and developing the Engineers. What We're Looking For ✅ A team player with excellent communication skills and the ability to train, coach and assist operators and other engineers. ✅ A Higher National Certificate (HNC) in an electrical, automation or multiskilled engineering discipline is desirable, supported by suitable ### Director, Quality Control - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $215K-$253K - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6016295004 - Excerpt: Director, Quality Control Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The position will provide strategic and organizational leadership for the Quality Control function supporting Corcept's development and commercial programs. This position will have end-to-end oversight of all stability programs at contract laboratories and will author the stability sections of regulatory filings. This position will partner closely with the Sr Director of Analytical Development & Quality Control (ADQC) to continuously strengthen, expand, and scale the QC function, with increasing responsibility across broader QC activities. Responsibilities: - Lead the QC function with primary responsibility for the design, execution, and oversight of stability programs - Oversee stability studies conducted at external laboratories, ensuring compliance, data integrity, and timely execution - Review, trend, and maintain stability data. Alert the project team of any adverse trending - Collaborate with vendors and internal cross-functional teams to ensure that out-of-trend and out-of-specification results are addressed promptly ### Logistics FLM - Associated British Foods - Location: Stoke (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://careers.abfgrocery.com/AlliedBakeries/job/Stoke-Logistics-FLM-ST5-9HT/3418-en_GB/ - Excerpt: Logistics FLM Stoke Overview of role 🚛 Drive Your Career Forward with Allied Bakeries! 📍 Location: Allied Bakeries Stoke (Newcastle-under-Lyme) 🕙 Hours: 4 on 4 off days and nights, 42 hours 💰 Salary: Competitive Are you a dynamic leader who thrives in a fast-paced environment where no two days are the same? We have an exciting opportunity for an experienced Logistics FLM to join our team at Allied Bakeries Stoke and lead the way in delivering excellence! As the Logistics FLM, you'll play a crucial role in ensuring that our products are safely delivered to customers on time and in full. Working under the guidance of the Logistics Manager, you'll inspire and motivate our Transport and Despatch teams, drive change, and implement improvements across the department. Key Accountabilities 🔹 Safety First: Lead by example and promote a culture of safety, ensuring all Health & Safety standards are met and maintained. 🔹 Team Leadership: Set clear goals, targets, and expectations for your team while motivating and supporting them to exceed objectives. 🔹 Training & Development: Help recruit, train, and develop staff to align with the company's values and goals, ensuring a high-performing team. 🔹 Continuous Improvement: Implement best practices and industry standards to improve operational efficiency, reduce costs, and enhance service levels. 🔹 Customer Satisfaction: Ensure that all despatched goods meet customer expectations, and manage compliance with traceability and food safety standards. 🔹 Cost Control: ### Senior Specialist, Regulatory Operations - Tonix Pharmaceuticals Holding Corp - Location: Frederick, MD (unspecified) - Salary: $70K-$130K - Posted: 2026-01-15 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4106035009 - Excerpt: Senior Specialist, Regulatory Operations Frederick, MD Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview The Senior Specialist, Regulatory Operations, will ### Quality Systems Manager - Associated British Foods - Location: Stoke (onsite) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://careers.abfgrocery.com/AlliedBakeries/job/Stoke-Quality-Systems-Manager-ST5-9HT/3719-en_GB/ - Excerpt: Quality Systems Manager Stoke Overview of Role 📍 Location: Newcastle-under-Lyme 🏠 Place of Work: Allied Bakeries Stoke (full- time on site role) 💰 Salary: Competitive ⏳ Hours: 37.5 hours across Monday-Friday, office hours Are you an experienced technical professional looking for your next challenge? We're hiring a Quality Systems Manager for our bakery site in Stoke to lead a team of quality auditors, provide advice to the site teams on all statutory regulations and company standards relating to food safety, quality and environmental hygiene to maximise the quality of our products. 📌 Your Role 🔹 You'll work closely with the central technical team to implement and share best practice at site; advising on all matters of food safety and legality in consultation with the Technical Manager. 🔹 Ensure that quality management systems, operating practices and process controls are developed, implemented and followed to ensure adherence to company site standards, consistent quality performance and hygiene standards. 🔹 Lead and advise the site teams on statutory regulations and company standards relating to food safety, quality and environmental hygiene including leading the site's HACCP and Internal auditing processes. 🔹 Develop initiatives which enhance the manufacturing operation through reduced costs and improved quality particularly in areas such as process monitoring & control. 🔹 Support the Technical Manager with all NPD and EPD introduction into site, delivering compliance to product specifications. 🔹 Ensure ### Maintenance Engineer - Associated British Foods - Location: Stoke (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://careers.abfgrocery.com/AlliedBakeries/job/Stoke-Maintenance-Engineer-ST5-9HT/3962-en_GB/ - Excerpt: Maintenance Engineer Stoke Overview of role 📍 Location: Allied Bakeries Stoke (Newcastle-under-Lyme) 🕙 Hours: 4 on 4 off, 2 days 2 nights (12 hour shifts) 💰 Salary: £52,886.22 Join Our Team! We have an excellent career opportunity for an experienced Maintenance Engineer to join our team in Stoke.The role of a Maintenance Engineer is a varied and challenging one. You will be expected to identify and deliver continuous improvement initiatives alongside proactive and reactive maintenance and repairs to the plant and site services associated with a major bakery. What You'll Be Doing 🔹Focusing on safe working practices and site performance KPI's including OEE and CCOs. 🔹Diagnosing and correcting automation, electrical and mechanical issues to resolve breakdown situations. 🔹Ensuring our engineering strategy is delivered consistently. 🔹Delivering turn-key improvement projects in a timely and cost-efficient manner. 🔹Driving the performance of the Engineering function forward. What We're Looking For Safety always comes first at Allied Bakeries. We are looking for someone to lead by example by ensuring that Health and Safety is the number one priority and engage others to always think and behave safely. ✅ A team player with excellent communication skills and the ability to train, coach and assist operators and other engineers. ✅ A Higher National Certificate (HNC) in an electrical, automation or multiskilled engineering discipline is desirable, supported by suitable experience. ✅ An enthusiastic and motivated in ### Hub Manager Stoke - Goodyear TIRE & Rubber - Location: GB Field Sales (unspecified) - Salary: Not disclosed - Posted: 2026-05-24 - 401(k) match: listed (not source-backed) - Apply: https://goodyear.wd1.myworkdayjobs.com/GoodyearCareers/job/GB-Field-Sales/Hub-Manager-Stoke_JR-40107970 - Excerpt: Hub Manager Stoke GB Field Sales Hub Manager Stoke Location: Newcastle-under-Lyme About Goodyear We're dedicated to producing, innovating, and servicing the best tires in the world. For over 125 years, Goodyear has led the way in developing smart solutions that shape the future of mobility. Today, we're one global team united by bold thinking, relentless drive, and a passion to exceed expectations. If you're ready to embrace change and make an impact in your career, let's go. Why This Role Matters This role plays a key part in delivering safe, efficient and high-quality TruckForce commercial tyre services across the territory. You will ensure our hubs, spokes and mobile operations run smoothly, safely and consistently, while creating an environment where teams feel supported, developed and empowered to do their best work. By balancing operational excellence, customer care and commercial performance, you help ensure we deliver outstanding service to fleet and local customers while strengthening long-term relationships and trust. Safety, continuous improvement and people development sit at the heart of everything you do. What You'll Do Lead and continuously improve operational performance across hub, spokes and van operations Champion a strong safety culture, ensuring all incidents are reported correctly and preventative practices are embedded Deliver excellent customer service across fleet inspections, fitments and account management, aligned to SLAs Oversee commercial performance including sales, profitability, margins and cost control Manage stock effectively, reducing waste, minimising slow-moving/obsolete stock and ensuring availability Support accurate and timely billing, credit control processes and reduction of aged debt ### Director, Regulatory Strategy - Rapport Therapeutics Inc - Location: 99 High Street, Suite 2100 , Boston, MA 02110 (unspecified) - Salary: $220K-$240K - Posted: 2026-01-24 - Apply: https://www.rapportrx.com/careers-board/?gh_jid=5001273007 - Excerpt: Director, Regulatory Strategy 99 High Street, Suite 2100 , Boston, MA 02110 When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we're driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we're doing this with extraordinary science and awesome people (affectionately called Rapptors). Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies. We are excited about the potential of our lead program, RAP-219. Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder. The strength of Rapport comes from our Rapptors - who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you're as excited about this opportunity as we are! Your Impact: The Director of Regulatory Strategy will play a pivotal role in leading strategic regulatory initiatives for assigned drug development programs. Your Day-to-Day: - Create and implement innovative and effective regulatory strategies to support the development of Rapport global drug development programs - Provide regulatory expertise and advise to cross-functional team ### Manager, Patient Safety & PV Compliance, Standards, and Training - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $160K-$200K - Posted: 2026-04-24 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5981632004 - Excerpt: Manager, Patient Safety & PV Compliance, Standards, and Training Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Manager, Patient Safety & Pharmacovigilance (PSPV) Compliance, Standards, and Training is responsible for supporting and managing activities for the execution and day-to-day oversight of PSPV compliance activities, including metrics/KPIs, maintenance of procedures, training programs, and quality system processes supporting both investigational and marketed products. This role partners closely with PSPV sub-functions, Quality Assurance, Clinical, Regulatory, and external vendors to ensure ongoing regulatory compliance. Key Responsibilities - Support operation and maintenance of the PSPV Quality Management System (QMS), ensuring procedures and processes are implemented consistently and in alignment with regulatory requirements - Author, review, revise, and maintain PSPV procedures, work instructions, and related controlled documents in compliance with global PV regulations (FDA, EMA, ICH) - Contribute to and manage activities for the development, implementation, and maintenance of role-based PV training programs, including initial ### Bakery Operative - Associated British Foods - Location: Stoke (unspecified) - Salary: GBP 29K-32K - Posted: 2026-06-12 - Apply: https://careers.abfgrocery.com/AlliedBakeries/job/Stoke-Bakery-Operative-ST5-9HT/3954-en_GB/ - Excerpt: Bakery Operative Stoke Overview of role Join Our Team: We are seeking Bakery Operatives to join our production team. We are looking for motivated and hardworking Bakery Operatives to join our fast-paced production team in Newcastle-Under-Lyme. If you enjoy hands-on work and want to build a career in food manufacturing, this could be the perfect oppertunity for you! 📍 Location: Allied Bakeries, Newcastle-under-Lyme. 💰 Salary: Starting at £28,791.60 increasing to £32,172.07 after successful completion of training. 🕙 Shifts: Average if 42 hours per week. This role operates 12-hour rotating shifts, on a varied shift pattern, including night work and weekends. What You Need To Know: As a Bakery Operative, you will play a key role in producing high-quality bakery products within a busy and highly regulated manufacturing environment. 🔹Engage in the Safety First culture and compliance with AB internal policies and procedures 🔹Maintain high standards of hygiene, safety and housekeeping 🔹Monitor product quality and consistency 🔹Support the efficient operation of production lines 🔹Take part in training and development activities, including 1-to-1 sessions This is a physically demanding role in a fat-paced factory enviroment, so resilience, reliability, and a positive attitude are essential. The Right Person Essential ✅ Good awareness of Health, Safety and Food Safety ✅ Basic numeracy and literacy skills, including record keeping and following instructions ✅ A positive can-do attitude, with a willingness to le ### Director, Regulatory Affairs - Infectious Disease - Tonix Pharmaceuticals Holding Corp - Location: Berkeley Heights, NJ (unspecified) - Salary: $150K-$240K - Posted: 2026-03-11 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4180874009 - Excerpt: Director, Regulatory Affairs - Infectious Disease Berkeley Heights, NJ Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position Overview The Director, Regulatory ### Director of Process Validation - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-09 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4075036 - Excerpt: Director of Process Validation Viking Therapeutics, Inc. Director of Process Validation ### Director, Thought Leader Liaisons - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $191K-$253K - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6015489004 - Excerpt: Director, Thought Leader Liaisons Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director, Thought Leader Liaisons is responsible for national leadership, strategic planning, and execution excellence for Corcept's TLL organization. This team engages thought leaders across endocrinology, diabetology, cardiology, nephrology, radiology, endocrine surgery, and other specialties to advance disease-state awareness, scientific education, and clinical insight generation. The Director partners extensively with Key Account Managers (KAMs), Clinical Specialists (CSs), Medical Science Liaisons (MSLs), Marketing, Field Medical, and Medical Affairs to ensure coordinated execution, consistent scientific engagement, and strong alignment with organizational priorities. Responsibilities: Strategic Leadership & Team Development - Lead, coach, and develop a high-performing national TLL team grounded in scientific excellence and collaboration - Establish strategic priorities, objectives, and KPIs aligned to corporate goals - Strengthen capabilities in scientific exchange, KOL engagement, insight capture, meeting facilitation, and peer-level clinical discussion - Ensure consistent field standards and best practices National ### Drug Safety Manager - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-03-19 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4014908 - Excerpt: Drug Safety Manager Viking Therapeutics, Inc. Drug Safety Manager ### Clinical Sales Specialist (CS) - Brooklyn, NY - Corcept Therapeutics - Location: Brooklyn, New York, United States (unspecified) - Salary: $140K-$155K - Posted: 2025-11-10 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5704575004 - Excerpt: Clinical Sales Specialist (CS) - Brooklyn, NY Brooklyn, New York, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The CS is accountable for implementing the sales strategies for approved products consistent with Corcept's compliance standards as well as all applicable legal requirements for those key targeted health care providers and hospital systems within an assigned territory. Responsibilities: - Build and develop professional relationships with influential high prescribers and thought leaders in the territory to enhance Corcept brand and product loyalty - Leverages expertise and knowledge of the therapeutic disease state, the marketplace, applicable competitors, industry, and cross-functional activities/plans to anticipate and effectively manage business opportunities and challenges - Develops and implements effective customer specific territory plans and communicates insights to internal stakeholders - Prioritizes time and effort to ensure optimal coverage of appropriate physician specialists based on opportunity and potential - Plan and participate in education programs and speaker dinner programs - Manage ### Clinical Trial Manager - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-05-11 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/3913773 - Excerpt: Clinical Trial Manager Viking Therapeutics, Inc. Clinical Trial Manager ### Senior/Staff Product Designer - Grow Therapy - Location: New York City, New York, United States, San Francisco, Seattle (unspecified) - Salary: $182K-$230K - Posted: 2025-07-08 - Mental health support: yes (not source-backed) - Apply: https://jobs.ashbyhq.com/grow-therapy/b2ff7626-cd25-4f2a-851c-6b77345209a5 - Excerpt: Senior/Staff Product Designer New York City, New York, United States, San Francisco, Seattle Grow Therapy is on a mission to serve as the trusted partner for therapists growing their practice, and patients accessing high-quality care. Powered by technology, we are a three-sided marketplace that empowers providers, augments insurance payors, and serves patients. Following the mass increase in depression and anxiety, the need for accessibility is more important than ever. To make our vision for mental healthcare a reality, we're building a team of entrepreneurs and mission-driven go-getters. Since launching in February 2021, we've empowered more than ten thousand therapists and hundreds of thousands of clients across the country and insurance landscape. We've raised more than $328Mm in funding, including our Series D, at a $3B valuation from Sequoia Capital, Transformation Capital, TCV, SignalFire, Menlo Ventures, Goldman Sachs Alternatives, and others. The Opportunity: We're seeking a Senior or Staff Product Designer to join our growing Design team and help shape the future of mental health technology. This is a senior-level role for an experienced designer ready to take on significant ownership and influence. You'll have the unique opportunity to work on 0-to-1 products that directly impact millions of users seeking mental health support, while operating at the intersection of product strategy, brand excellence, and user experience to create breakthrough solutions in a rapidly evolving industry. What You'll Be Doing: - Drive strategic product initiatives from concept to launch, leveraging design thinking to influence product strategy and business outcomes - Design and ### Medical Science Liaison Director/Lead - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-27 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4116882 - Excerpt: Medical Science Liaison Director/Lead Viking Therapeutics, Inc. Medical Science Liaison Director/Lead ### Director, Regulatory Affairs CMC - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $239K-$281K - Posted: 2026-02-05 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5795300004 - Excerpt: Director, Regulatory Affairs CMC Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . Lead the preparation of CMC Regulatory documents from pre-IND to marketing authorization submissions in multiple therapeutic areas, molecules, and regions. This position will lead direct reports in the CMC regulatory team, keep up to date on evolving regulations, and lead regulatory intelligence activities. This is a hybrid role that typically requires on-site presence three days per week. Responsibilities: - Effectively maintain, and motivate a high-performing regulatory CMC team, including developing, coaching, and mentoring diverse, talented, and driven staff - Lead regulatory - CMC intelligence activities - Lead regulatory CMC activities for assigned projects consistent with global regulatory requirements , and company policies and procedures - Provide Regulatory CMC guidance to internal teams and lead cross-functional teams to plan and prepare briefing packages, and CMC sections for INDs, and equivalent IMPD sections for CTAs, NDAs/MAAs and other global submissions ### Associate Director, Formulation Development - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4079847 - Excerpt: Associate Director, Formulation Development Viking Therapeutics, Inc. Associate Director, Formulation Development ### Senior/Executive Director, Health Economics & Outcomes Research (HEOR) - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-29 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4127771 - Excerpt: Senior/Executive Director, Health Economics & Outcomes Research (HEOR) Viking Therapeutics, Inc. Senior/Executive Director, Health Economics & Outcomes Research (HEOR) ### Associate Director, Regulatory Affairs - Kalvista Pharmaceuticals INC - Location: Salisbury, UK (unspecified) - Salary: Not disclosed - Posted: 2026-04-23 - Apply: https://job-boards.greenhouse.io/kalvistapharmaceuticals/jobs/5198828008 - Excerpt: Associate Director, Regulatory Affairs Salisbury, UK About KalVista Pharmaceuticals, Inc. KalVista is a global pharmaceutical company dedicated to delivering life-changing oral therapies for individuals affected by rare diseases with significant unmet needs. The KalVista team discovered and developed EKTERLY®-the first and only oral on-demand treatment for hereditary angioedema (HAE)-and continues to work closely with the global HAE community to improve treatment and care for this disease around the world. For more information about KalVista, please visit www.kalvista.com and follow us on LinkedIn , X , Facebook and Instagram . ABOUT THE ROLE The Associate Director, Regulatory Affairs will join the Regulatory Development team at KalVista in contributing to the development of regulatory submissions in alignment with company objectives and support the successful commercialization of KalVista's products. The position provides regulatory expertise and guidance across both pre and post approval activities, serving as the regulatory lead for designated territories. Responsibilities include ensuring ongoing regulatory compliance within those territories while partnering cross-functionally to support strategic and operational regulatory requirements. RESPONSIBILITIES Support IND/NDA/MAA preparation, submissions, assessment and post approval activities in designated territories, in close collaboration with the Global Regulatory Lead Represent regulatory affairs in allocated launch teams as required Provide regulatory support to business development, commercial, market access, pharmacovigilance, supply chain and quality functions Working closely with other regulatory team members, to draft/put in place appropriate processes (SOPs) to ensure ongoing maintenance/regulatory compliance of marketing authorizations in designated markets Contribute to KalVista's Regulatory Intelligence process Maintain compliance with KalVista's Quality Management System ### Senior Therapeutic Area Specialist, Neuroscience - Cobenfy - Fort Worth, TX - Bristol Myers Squibb - Location: Fort Worth - TX - US (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Fort-Worth---TX---US/Senior-Therapeutic-Area-Specialist--Neuroscience---Cobenfy---Fort-Worth--TX_R1601235 - Excerpt: Senior Therapeutic Area Specialist, Neuroscience - Cobenfy - Fort Worth, TX Fort Worth - TX - US posted: Posted 7 Days Ago ### Therapeutic Mentor - Centerstone - Location: Bradenton, Florida (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://centerstone.wd5.myworkdayjobs.com/CenterstoneCareers/job/Bradenton-Florida/Therapeutic-Mentor_JR-030233 - Excerpt: Therapeutic Mentor Bradenton, Florida posted: Posted 2 Days Ago ### Associate Director, Pipeline & Portfolio Market Planning - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $215K-$253K - Posted: 2026-04-27 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5982908004 - Excerpt: Associate Director, Pipeline & Portfolio Market Planning Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Associate Director, Pipeline and Portfolio Market Planning is accountable for developing product strategies across Corcept's oncology portfolio. This individual will guide indication selection and sequencing, competitive landscape assessments, target product profiles (TPPs), product proposition, and long-range financial forecasting to inform program-level decision-making . Responsibilities: - Lead program-level strategy initiatives to define product vision, optimize lifecycle value, and drive business impact - Provide integrated physician, patient, and payer perspective in clinical strategy and new product planning initiatives - Own the design, implementation, and continuous refinement of competitive intelligence and market analysis frameworks that proactively inform program, investment, and governance decisions - Support cross-functional teams, including Commercial, Medical, Development, and Research, to ensure alignment and strategic continuity across the product lifecycle - Develop, maintain, and communicate long-range revenue forecasts and valuation models to support program planning ### Vice President, Commercial Manufacturing Operations - VERA Therapeutics INC - Location: Remote (remote) - Salary: $248K-$375K - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4273981009 - Excerpt: Vice President, Commercial Manufacturing Operations Remote Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics' mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics' lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell-mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit www.veratx.com . Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do-from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases. Position Summary: The Vice President, Manufacturing Operations will report ### VP, Clinical Development - Infectious Disease - Tonix Pharmaceuticals Holding Corp - Location: Frederick, Maryland or Berkeley Heights, New Jersey (unspecified) - Salary: $250K-$350K - Posted: 2026-01-20 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/tonixpharmaceuticals/jobs/4108447009 - Excerpt: VP, Clinical Development - Infectious Disease Frederick, Maryland or Berkeley Heights, New Jersey Tonix Pharmaceuticals* is a fully integrated, commercial-stage biotechnology company focused on central nervous system (CNS) and immunology treatments in areas of high unmet medical need. TONMYA® (cyclobenzaprine HCl sublingual tablets 2.8 mg) is the first new treatment for fibromyalgia in adults in more than 15 years. Tonix's CNS commercial infrastructure supports its marketed products, including its acute migraine products, Zembrace® Symtouch® (sumatriptan injection 3 mg) and Tosymra® (sumatriptan nasal spray 10 mg). Tonix is investigating TONMYA® in Phase 2 clinical trials to evaluate its potential in major depressive disorder and acute stress disorder/acute stress reaction. Tonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. In addition, the Company is progressing TNX-2900 (intranasal potentiated oxytocin), which is Phase 2 ready for the treatment of Prader-Willi syndrome, a rare disease. To learn more, visit www.tonixpharma.com and follow the Company on LinkedIn and X . *Tonix's product development candidates are investigational new drugs or biologics; their efficacy and safety have not been established and have not been approved for any indication. Zembrace SymTouch and Tosymra are registered trademarks of Tonix Medicines. TONMYA is a registered trademark of Tonix Pharma Limited. All other marks are property of their respective owners. Position ### Therapeutic Specialist - Gilead Sciences - Location: Spain - Alicante (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Spain---Alicante/Therapeutic-Specialist_R0052600 - Excerpt: Therapeutic Specialist Spain - Alicante posted: Posted 2 Days Ago ### Clinical Sales Specialist (CS) - Atlantic City, NJ - Corcept Therapeutics - Location: Atlantic City, New Jersey, United States (unspecified) - Salary: $140K-$155K - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6016738004 - Excerpt: Clinical Sales Specialist (CS) - Atlantic City, NJ Atlantic City, New Jersey, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The CS is accountable for implementing the sales strategies for approved products consistent with Corcept's compliance standards as well as all applicable legal requirements for those key targeted health care providers and hospital systems within an assigned territory. Responsibilities: - Build and develop professional relationships with influential high prescribers and thought leaders in the territory to enhance Corcept brand and product loyalty - Leverages expertise and knowledge of the therapeutic disease state, the marketplace, applicable competitors, industry, and cross-functional activities/plans to anticipate and effectively manage business opportunities and challenges - Develops and implements effective customer specific territory plans and communicates insights to internal stakeholders - Prioritizes time and effort to ensure optimal coverage of appropriate physician specialists based on opportunity and potential - Plan and participate in education programs and speaker dinner programs ### Therapeutic Specialist I - Gilead Sciences - Location: China - Kunming (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Kunming/Therapeutic-Specialist-I_R0052372-2 - Excerpt: Therapeutic Specialist I China - Kunming posted: Posted 30+ Days Ago ### Senior Director, Executive & Enterprise Communications - Revolution Medicines - Location: Redwood City, California, United States (unspecified) - Salary: $244K-$305K - Posted: 2026-05-01 - 401(k) match: listed (not source-backed) - Apply: https://www.revmed.com/careers-list/?gh_jid=7613269003 - Excerpt: Senior Director, Executive & Enterprise Communications Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: The Senior Director, Executive & Enterprise Communications will serve as a trusted communications advisor to the CEO and select senior leaders while leading enterprise internal communications across a growing global organization. This is a high-impact role for a communicator who can operate strategically and execute with excellence. Success in this position requires sound judgment, executive presence, strong writing skills, and the ability to move seamlessly between shaping a CEO keynote and building the communications infrastructure that keeps teams informed, aligned, and engaged. Reporting to the Head of Communications, this role partners closely with the Corporate Communications lead, the Associate Director of Internal Communications, and regional communications and HR partners globally. This is a rare opportunity to work directly with RevMed's executive leadership team, shaping executive voice, internal culture, and enterprise communications at a company rapidly building toward commercial stage. Key responsibilities ### Therapeutic Specialist II - Gilead Sciences - Location: China - Shenyang (unspecified) - Salary: Not disclosed - Posted: 2026-05-19 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Shenyang/Therapeutic-Specialist-I_R0051136-1 - Excerpt: Therapeutic Specialist II China - Shenyang posted: Posted 24 Days Ago ### Senior Therapeutic Specialist - Gilead Sciences - Location: Norway - Oslo (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Norway---Oslo/Senior-Therapeutic-Specialist_R0052304-1 - Excerpt: Senior Therapeutic Specialist Norway - Oslo posted: Posted 30 Days Ago ### Executive Director / Vice President, Corporate and Internal Communications - BioPharma - Dianthus Therapeutics - Location: Remote (remote) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/dianthustherapeutics/jobs/4679135005 - Excerpt: Executive Director / Vice President, Corporate and Internal Communications - BioPharma Remote About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology - enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation - enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections. To learn more, please visit www.dianthustx.com and follow us on LinkedIn . About the Role BioPharma Experience is required. We are seeking a strategic, creative, and execution-oriented ED / VP, Corporate & Internal Communications to build and lead a modern, high-impact communications function in a fast-growing biotech company. This role sits at the intersection of people, corporate brand, and business strategy-responsible for shaping how we communicate internally and externally, strengthening employee engagement, elevating our corporate brand, and ensuring a consistent and compelling company narrative across all audiences, while operating as predominantly a remote company. You will serve as a trusted advisor to senior leadership and partner closely with the VP of Marketing and VP of Investor Relations to ensure alignment across corporate and internal communications. We are building a culture of individuals who hold our core principles at ### Clinical Sales Specialist (CS) - Jacksonville South - Corcept Therapeutics - Location: Jacksonville, Florida, United States (unspecified) - Salary: $140K-$155K - Posted: 2025-04-29 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5529809004 - Excerpt: Clinical Sales Specialist (CS) - Jacksonville South Jacksonville, Florida, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The CS is accountable for implementing the sales strategies for approved products consistent with Corcept's compliance standards as well as all applicable legal requirements for those key targeted health care providers and hospital systems within an assigned territory. Responsibilities: - Build and develop professional relationships with influential high prescribers and thought leaders in the territory to enhance Corcept brand and product loyalty - Leverages expertise and knowledge of the therapeutic disease state, the marketplace, applicable competitors, industry, and cross-functional activities/plans to anticipate and effectively manage business opportunities and challenges - Develops and implements effective customer specific territory plans and communicates insights to internal stakeholders - Prioritizes time and effort to ensure optimal coverage of appropriate physician specialists based on opportunity and potential - Plan and participate in education programs and speaker dinner programs - Manage territory --- Source-backed benefit claims include source links; other benefit values are labeled separately.