Crinetics Pharmaceuticals INC jobs

Senior Manager, Clinical Data Management - External Data Management Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Manager, Clinical Data Management - External Data Management (CDM‑EDM) is a hands‑on, individual contributor role responsible for executing and owning external (non‑EDC) data management activities for assigned clinical studies. This position focuses on direct execution and plays a critical role in ensuring external vendor data are timely, high quality, inspection‑ready, and fit for statistical analysis and regulatory submission. The role partners closely with external vendors, CROs, and internal cross‑functional stakeholders to set up data transfer agreements (DTAs), validate test files, manage ongoing data transfers, and perform data reconciliation and quality control activities in compliance with ICH‑GCP, 21 CFR Part 11, and internal SOPs. Essential

Senior Medical Director, Clinical Research, Endocrinology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Medical Director, Clinical Research will be working within a multi-disciplinary team and will be accountable for developing the strategy and the Clinical Development Plan for one or more indications for a specific Crinetics' compound. The incumbent will have hands-on responsibility designing, executing, and analyzing clinical trials. The incumbent will have a key role in the understanding and interpretation of the results from these studies as well as the preparation of the summary documents needed for a global submission to regulatory authorities. Essential Job Functions and Responsibilities: These may include but are not limited to: Clinical leader of one or more endocrinology programs, being integral to developing the

Vice President, Drug Safety/Pharmacovigilance Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Vice President of Drug Safety/Pharmacovigilance will be instrumental in supporting the growth of the organization as it continues to build the value of its current products and develop new products. The incumbent will design and develop the Global Crinetics Drug Safety and Pharmacovigilance system, ensuring adequate resourcing, efficient and compliant safety reporting, designing implementation of Safety Surveillance Programs, oversight of the safety profiles of Crinetics products and playing a leading role in safety risk management activities. Essential Job Functions and Responsibilities: These may include but are not limited to: Safety reporting processes. Ensure the accurate receipt and processing of safety assessment reports. Ensure that medical and causality assessments of all

Associate Director, in Vivo Pharmacology San Diego, CA Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Associate Director, In Vivo Pharmacology, will be responsible for providing in vivo pharmacology support to Endocrine Discovery teams including designing, conducting, and interpreting experiments to demonstrate efficacy and evaluate safety of novel nonpeptides in animal models. The candidate will have a broad background in in vivo pharmacology and will contribute to several preclinical programs as well as the identification of new therapeutic targets. Essential Job Functions and Responsibilities: These may include but are not limited to: Lead the Endocrine Discovery In Vivo Pharmacology team to plan, design, conduct, and interpret in vivo experiments to evaluate the efficacy, pharmacokinetics, and safety of therapeutic candidate molecules in support

Vice President, Clinical Research Endocrinology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: Crinetics is seeking an experienced, strategic, dynamic, and innovative Vice President of Endocrinology Clinical Research reporting to the Chief Medical Officer (CMO). The Vice President Clinical Research Endocrinology will be instrumental in further building and developing the Endocrinology Clinical Research function at Crinetics. In collaboration with the executive leadership (CMO), the vice president will serve as a deputy for the CMO and provide support to drive clinical development for Crinetics endocrinology drug candidates and provide clinical guidance to support the discovery of new endocrinology drug candidates. The incumbent will collaborate across the organization to identify, develop, and deliver life-changing therapies to people living with endocrinology disorders and their complications. Essential

Vice President, Total Rewards and HR Operations San Diego, CA Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors . We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Vice President, Total Rewards & HR Operations will strategically lead the Compensation, Benefits, and HR Operations functions within the Human Resources department. Reporting to the Chief Human Resources Officer, this role is accountable for evolving Crinetics' total rewards philosophy and programs to support the company's continued growth and increasing organizational complexity. This leader will serve as an internal subject matter expert for compensation, benefits, wellness, HR operations, and HR systems; drive scalable, compliant processes and controls; and build a high-performing team and operating model that deliver exceptional employee experience in a complex, multi-state environment. Essential Job Function s and Responsibilities : These may

Contract Manager San Diego, CA Position Summary: The Crinetics Legal Team is seeking an experienced Contracts Manager to support Technical Operations (formerly CMC) and broader G&A functions. This role serves as a key business partner to Technical Operations, enabling efficient, compliant, and scalable contracting across development, manufacturing, supply chain, and quality operations. This individual will manage a high volume of contracts with external partners, including Contract Manufacturing Organizations (CMOs), Contract Development and Manufacturing Organizations (CDMOs), suppliers, and service providers. Core responsibilities include drafting, reviewing and negotiating a range of agreements, including but not limited to Master Service Agreements (MSAs), Statements of Work (SOWs), supply and technical services agreements, consulting agreements, and related amendments and change orders. In addition to contract execution, this role will play a critical part in supporting and enabling business stakeholders, including guiding end users through the contract intake process, improving submission quality, and providing training on contracting processes and tools (e.g., Ironclad CLM). The role will also support contract processes tied to GxP compliance, regulatory inspections, and product lifecycle activities, ensuring alignment with company policies and regulatory requirements. This position will contribute to the ongoing maturity and optimization of the end-to-end contracting lifecycle, including process improvements, template standardization, and stakeholder enablement. Essential Job Functions and Responsibilities: These may include but are not limited to: Lead the preparation, review, and negotiation of contracts, ensuring all key terms, including scope, deliverables, milestones, timelines, and termination provisions, are clearly defined, accurately tracked, and aligned with business objectives. Partner cross-functionally

Senior Clinical Research Associate Remote Position Summary: The Senior Clinical Research Associate (Sr. CRA) will participate in the preparation and execution of Phase 1-3 clinical trials. The Sr. CRA oversees the progress of clinical investigations by conducting site qualification, initiation, interim, and close-out visits. The Sr. CRA monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by Crinetics Pharmaceuticals and partner CRO(s). The Sr. CRA works closely with the Clinical Trial Manager (CTM) and Clinical Monitoring management to ensure all monitoring activities are conducted according to study requirements. The Senior CRA may also participate in monitoring oversight activities such as CRO oversight visits, internal CRA training and evaluation visits, and CRO monitoring visit report review. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop strong, collaborative investigational site relationships and ensure continuity of relationships through all stages of the trial. Perform clinical study site management/monitoring activities efficiently in compliance with GCP/ICH requirements, SOPs, local laws and regulations, protocol, Clinical Monitoring Plan, and associated documents. Participate and provide input on site selection and site qualification activities. Coordinate and manage assigned tasks in collaboration with the study team to achieve site activation. Perform remote and on-site monitoring activities using various tools to ensure subject rights, safety and well-being are protected as well as the reliability and integrity of study data. Conduct site visits including but not limited to qualification visits, initiation visits, interim monitoring visits, and close-out visits; generate clear, comprehensive, and accurate

Associate Manager, Centralized Monitoring Remote Position Summary: The Associate Manager, Centralized Monitoring is responsible for executing and overseeing centralized monitoring activities across clinical trials using a risk-based quality management (RBQM) framework. The role focuses on proactive signal detection, data surveillance, risk identification support, and escalation to support study quality, participant safety, and regulatory compliance. This position also contributes to process improvement, and cross-functional collaboration related to centralized monitoring activities. Incumbent will support cross-functional collaboration across multiple clinical studies, with a focus on regulatory compliance and inspection readiness. Essential Job Functions and Responsibilities: These may include but are not limited to: Support the execution of centralized monitoring strategies for studies ensuring setup aligns with Crinetics' RBQM best practices. Perform ongoing centralized monitoring reviews using clinical, operational, and quality data sources (e.g., EDC, CTMS, safety, vendor data). Identify emerging study-level and site-level risks through Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and analytical outputs. Support the evaluation of trends, data anomalies, protocol deviations, and performance metrics to detect potential quality or compliance issues. Document and report signals, findings, and recommendations within designated systems (e.g., CTMS, RBQM platform). Support study teams' understanding of the significance and root causes of centralized monitoring findings. Contribute to the development and maintenance of RBQM documentation, including: Centralized Monitoring Plans KRI and QTL threshold definitions SDV and SDR strategies Collaborate with Clinical Monitoring to support alignment of monitoring approaches with ICH-GCP E6 (R2/R3) and internal SOPs. Provide input on targeted monitoring actions, such as focused SDV, site

Director, Corporate Compliance San Diego, CA Position Summary: As a leader and a trusted Business Partner, the Director of Corporate Compliance will have overall responsibility for the commercial and medical affairs teams by providing timely compliance advice and measured guidance as a strategic business partner ensuring compliance requirements are integrated into business processes. This role is critical to fostering a culture of compliance throughout the organization while enabling the organization to make informed decisions to meet long-term goals. Essential Job Functions and Responsibilities: As the liaison between the compliance department and the commercial and medical affairs teams, this role will be responsible for achieving organizational objectives by effectively integrating into the business to drive compliant activity. These may include but are not limited to: Collaborate: Establish strong working relationships and act quickly to ensure timely thoughtful advice is provided to key business partners. Educate: Develop and deliver targeted training to enable informed decision making in support of the needs of the business unit. Monitor: Assess activities to ensure alignment with healthcare compliance requirements. Detect: Identify areas of compliance risk within respective business areas to ensure systems, processes, training and other resources are coordinated to help mitigate risk. Strategize: Embrace inherent risks associated within the industry and develop and implement strategies that recognize these risks as necessary for impactful innovation. Evaluate: Pursue options and evaluate strategies and technology to enhance business processes. Adapt: Adjust compliance strategies in response to regulatory changes, compliance trends and best practices while ensuring the organization remains

Senior Accountant 1 Remote Position Summary: The Senior Accountant 1 is responsible for helping to ensure the accuracy, completeness and appropriateness of general ledger transactions in accordance with US GAAP. Requires the ability to read and interpret contractual terms to ensure all costs associated with contractual commitments are recorded in the financial statements during the appropriate accounting period. This position will participate in a variety of financial functions including month-end closing, financial reporting and other administrative functions. Areas of responsibility will typically be in most challenging areas of the Company's accounting, including R&D accruals. A SOX-compliant mindset, strong, proactive, analytical, and problem-solving skills, and desire and ability to identify, recommend and lead improvements is important. Other duties include reviewing coding on invoices, maintaining banking records, reconciling BS schedules, and miscellaneous accounting and administrative duties . Essential Job Functions and Responsibilities: These may include but are not limited to: Support month-end close process, including data entry, reconciliation of sub-ledgers to the general ledger, and maintenance of balance sheet account reconciliations Prepare G&A, and select R&D accruals, including maintaining trackers, coordination with functional leaders and analyzing other accruals for accuracy and completeness Assist with operationalizing contract terms and ensuring appropriate accounting treatment in accordance with guidance assessed by the SEC & Technical Accounting team Manage prepaid reconciliations, including subscriptions, insurance and other prepaid accounts Oversee fixed asset accounting including additions, disposals, depreciation, and execution of the annual fixed asset inventory Prepare and record payroll‑related journal entries and partner closely with the Payroll

CRM Developer / Administrator United States Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space. Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity. I. Position Summary: Reporting to the Sr Director, Data Strategy & Analytics, this role is responsible for supporting the implementation and integrations of large data assets and analytics into the Ocular CRM. Work with the Sr Director, Data Strategy & Analytics to optimize all reporting platforms. The Sr Associate, Business Analytics must be able to work in a matrix organization to compliantly address the analytical needs of his/her internal customers. II. Principal Duties and Responsibilities include the following: - Lead configuration, customization, maintenance, and support in the effective assessment, development, delivery, and usage of Ocular's CRM application for Field Sales, Reimbursement and Medical teams. - Design, develop, deploy, provide end user support, and maintain dashboards, reports, user roles, security, profiles, workflow rules, etc. while integrating the team's business needs into Veeva CRM. -

Scientist II, Animal Model Development 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 Tonix Research and Development Center

Pharmaceutical Production Lead - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago

Technician, Pharmaceutical Sligo, SO, Ireland Company Description: About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 12 month fixed-term contract. This role is rotational shift work. In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements. A snapshot of your key responsibilities as a Pharmaceutical Technician would be: Pharmaceutical processing activities in our manufacturing building and support locations. Team co-ordination to maximise the effectiveness of the team members. Documentation of all activities in line with cGMP requirements. Cross training within the team and training of new team members. Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems. Execution of commissioning and validation protocols on an ongoing basis. Maintaining the overall cGMP of the pharmaceutical processing areas. Adheres

Pharmaceutical Manufacturer Relations Executive Remote Nationwide posted: Posted 2 Days Ago

CRNA - Strike Force Float CRNA-Houston Market- $352(k) for 44 Weeks Houston, TX We're looking for a service-oriented CRNA to join our Strike Force Team and float between our five facilities throughout Houston and Beaumont, TX. Position Highlights: - $352,000 for 44 Weeks of Service - Flexibility of weeks scheduled - 1099 Position - Float between 5 Houston Facilities + Beaumont, TX - NO CALL - Mix of hospital(s) and ASC's - Mileage Reimbursement - Guaranteed Hours - Malpractice and Tail Coverage Provided Qualifications: - Board Certified - 1 year or more of experience What We Offer - 352K 1099 - Flexible scheduling - Opportunity to pick up shifts for additional compensation - Ability to advance your skills and training - Paid Malpractice + tail - Support from our Corporate Clinical Leaders About Us: Essential Anesthesia Management, a partnership between YPS and EmergencHealth, is a clinician-founded, clinician-led anesthesia management company striving to deliver the highest quality anesthesia care to both patients and hospitals alike. Over the past several years, we have experienced significant growth, providing turn-key department management at over 125 facilities in 6 states. Over 1400 CRNA and Anesthesiologist providers make up the Essential Team. We are continually seeking additional service-minded professionals to join our team and pride ourselves on hiring the best and brightest. We want to hire exceptional people. If you want to be part of a great anesthesia team that really understands the day-to-day demands in the OR, please give us a call at 602-620-3037. Essential

Pharmaceutical Product Operator - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago

Pharmaceutical Production Technician - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago

CRM Clinical Specialist II | CDMX Benito Juárez, DF MX-CMX, Mexico | N/A

Pharmaceutical Information Specialist CHN - Shanghai - Shanghai (Tower A) posted: Posted 7 Days Ago

PRN - CRNA - The Physicians Centre Hospital - Bryan, TX | Award-Winning Facility! Ortho-Heavy! Bryan, Texas Essential Anesthesia Management is looking for a CRNA to join our team on a PRN basis at Physicians Centre Hospital in Bryan, Texas. Position Highlights: - $200/hr with malpractice covered - hours guaranteed! - CRNA-only facility; great opportunity to work with full autonomy! - Anesthesia team consists of 6 CRNAs - Physicians Centre is an ortho heavy site, but also services general surgery, bariatric, urology, ENT, spine, ophthalmology and pain management cases. No pediatric, OB, Heads or Hearts at this facility. - CRNAs are required to perform regional and peripheral nerve blocks - we are willing to train any provider that needs to increase block competency! - PCH is the recipient of the Joint Replacement Excellence Award and Total Knee Replacement Five-Start Recipient. We are looking for a strong CRNA to complete our tenured team! Qualifications: - Board certified - Proficient or willing to learn regional and peripheral nerve blocks. What We Offer: - Ability to work autonomously & continue to develop skills - Paid malpractice + tail - Financial coaching - Access to group benefits through preferred partnerships - Support from our Corporate Clinical Leaders About Bryan, TX: - The town's motto is the “Good Life, Texas Style,” and that perfectly accentuates this towns culture and vibe. Check out the town's website for more at https://www.bryantx.gov/ . - Bryan offers an affordable cost of living, high quality public schools, a strong sense

Pharmaceutical Information Manager CHN - Shanghai - Shanghai (Trading) posted: Posted 8 Days Ago

Clinical Trial Manager Remote Position Summary: The Clinical Trial Manager is responsible for managing the execution of clinical studies and data collection. The incumbent oversees the review, monitoring and adherence to clinical protocols, as well as fulfilling activities related to study completion. The Clinical Trial Manager will interact internally and externally with members of the cross-functional study team. Essential Job Functions and Responsibilities: These may include but are not limited to: Provide oversight of clinical research studies across all functional areas of the drug development process. Provide operational and strategic input into study documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Clinical Database edit specifications, Clinical Study Report (CSR) development, etc. Develop the subject recruitment/retention strategy and related initiatives. Oversight of TMF set-up, ongoing quality review, and final reconciliation of study documents including review of site regulatory documents/packages and obtaining of appropriate site insurance, and/or supervision of team members performing these activities. Development of training materials for study team, investigational sites, and vendors. Proactive management of information sharing with key stakeholders using standardized reports and other mechanisms. Assure clinical studies are compliant with ICH/GCP and other regulations as appropriate. Oversee preparation of RFPs and prepare bid templates to facilitate selection of the CROs/vendors, and/or collaboration/supervision with team members performing these activities. Collaborate with counsel to negotiate and draft research contracts and agreements with CROs/vendors and clinical study sites, as needed. Acts as liaison with Regulatory Affairs to assure adherence to GCPs;