Biocryst Pharmaceuticals INC jobs

Paralegal, Generalist 2 Locations COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY The Paralegal, Generalist provides broad-based legal and operational support across the Legal and Compliance function. This role supports contract lifecycle activities, manages discrete legal and compliance-related projects, and serves as a key coordination point between attorneys, business stakeholders, and external partners. The position operates in a highly collaborative and fast-paced, regulated environment. ESSENTIAL DUTIES & RESPONSIBILITIES Contracting & Legal Support Support the end-to-end contract lifecycle, including intake, tracking, drafting support, review coordination, execution, and archival of agreements. Prepare and manage standard form agreements (e.g., NDAs, employment agreements, separation agreements, consulting agreements, vendor agreements, amendments) using approved templates and playbooks. Coordinate contract review and approval workflows between attorneys, business owners, and external parties. Maintain contract records in contract management systems and shared repositories, ensuring accuracy, completeness, and version

Regional Business Director 7 Locations COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The Regional Business Director (RBD) will be responsible for the business performance and achievement of company objectives within the assigned region. The RBD will be accountable for designated region's P&L. Candidates must live NY, MA, NH, ME, CT, or NJ. #LI-REMOTE ESSENTIAL DUTIES & RESPONSIBILITIES: Responsible for exceeding goals and objectives for the respective region. Serve as member of the sales leadership team, ensuring alignment with goals and objectives of the commercial leadership team and the broader organization. Hire, lead, inspire, coach and develop the Rare Disease Specialists in respective region. Provide strategic direction to Rare Disease Specialists in order to exceed goals and objectives. Develop and maintain relationships with key customers within assigned region. Direct the development and execution of regional business plan and manage

Patient Support Manager - Southeast 3 Locations COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. ESSENTIAL DUTIES & RESPONSIBILITIES: Direct the access support between consented patients and all relevant stakeholders (Pharmacy, MDO, support organizations). Oversee quality-control efforts relating to Pharmacy interface with payers for consented patients. Direct and coordinate onboarding of all new consented patients. Manage patient status changes within Patient Services CRM and follow-up with internal stakeholders and pharmacy. Enforce Patient Support Program business rules to administer access to these programs. Manage and communicate reimbursement-related information to consented patients and MDOs Control the flow of information to and communication touch-points with consented patients. Support adherence efforts. Collaborate with Market Access to execute regional reimbursement patient educational events. Create and manage a comprehensive product access and patient support plan for consented patients. Lead the cross-functional execution activities. Lead weekly meetings with

Lab Technician - Res. Biology (Contract) US_Alabama_Discovery Center JOB SUMMARY: This position will contribute to early R&D programs and clinical biomarker study programs in our Discovery Center of Excellence in Birmingham, Alabama. The Lab Technician has overall responsibility to maintain the organization of the Biology lab including managing laboratory supplies, updating compounds/biology reagents/kits inventories, lab notebooks, and specific lab equipment. The incumbent will also perform assigned duties to assist principal investigators in performing routine lab work. ESSENTIAL DUTIES & RESPONSIBILITIES: Assists with early research and development program studies including method development and compound testing. Assists with pharmacodynamic (PD) biomarker studies including sample login, storage, and organization. Assists with biological and biochemistry assays for compound testing and biomarker assessment. Supports the biologics program including antibody receiving, login, aliquot, storage, and inventory management. Performs preventive maintenance on specific lab equipment. Prepare reagents for routine work performed. Responsible for organizing, storing and maintaining compounds, biology reagents and kits (inventory) and general lab supplies (assisting with day-to-day organization of the biology lab). Responsible for lab cleaning and organization. Responsible for organizing laboratory notebooks. Manages the receipt, verification, and routing of incoming laboratory shipments within the biology lab. Provides timely assistance whenever needed in the laboratory. EXPERIENCE & QUALIFICATIONS: Bachelor's degree in biology or any relevant science-related field is required. Experience working in a lab is preferred. Good organization skills, attention to details, and willingness to help other lab members are essential. Ability to communicate effectively at all levels in the organization, verbally and in

SVP, Pharmaceutical Sciences US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The SVP of Pharmaceutical Sciences (Pharm Sci) is responsible for PharmSci strategy and execution across both biologics and small molecules, including drug substance and drug product development, clinical supplies, scale-up and technology transfer, and analytical development. ESSENTIAL DUTIES & RESPONSIBILITIES: Align project priorities, coordinate PharmSci activities, project deliverables and resources between PharmSci and other Developmental functions in BioCryst Mentor and develop a high performing PharmSci leadership team that efficiently coordinates activities across different PharmSci functional areas. Maintain seamless collaboration with other functional areas of the organization to ensure project progress according to agreed timelines especially research and discovery. Work closely with Clinical, Quality, Regulatory, Technical Operations, Preclinical and Finance functions in the company in the development and execution of PharmSci plans to meet corporate objectives. Serve

Assoc. Director, Global Data Science Operations US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: We are seeking a highly motivated Data Scientist to join our Strategic Data Insights and Operations team. This role will support the development and execution of advanced analytics strategies across corporate, commercial, medical, and clinical domains. The ideal candidate will bring a strong foundation in data science, strong knowledge in machine learning, a passion for improving patient outcomes, and the ability to translate complex data into actionable insights that drive strategic decisions. ESSENTIAL DUTIES & RESPONSIBILITIES: Design and implement predictive models, machine learning algorithms, and statistical analyses to support business decisions across Commercial, Medical Affairs, and Clinical Operations. Integrate and analyze large-scale datasets, including anonymized patient-level data (APLD), real-world evidence (RWE), and internal operational data. Collaborate with cross-functional teams to define Key Performance

Sr. Toxicologist US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: We are seeking a highly organized and detail-oriented early-career scientist to join us in a cross-functional role serving as an integral liaison between BioCryst and Contract Research Organizations (CROs) serving predominantly as Study Monitor. The successful candidate will have a few years of direct experience as a Study Director at a Contract Research Organization with a focus in Toxicology studies as they apply to pharmaceutical development and will use this experience to provide oversight of BioCryst studies while liaising internally with BioCryst scientists to ensure seamless communication enabling the streamlining of scientific operations. ESSENTIAL DUTIES & RESPONSIBILITIES: Collaborate with nonclinical program leads and other subject matter experts to design nonclinical studies in alignment with program needs and regulatory requirements. Act as Study Monitor for Toxicology, Pharmacology, and/or

Exec. Director, Global Supply Chain Operations 2 Locations COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. ESSENTIAL DUTIES & RESPONSIBILITIES: Oversees all internal and external supply operations related to commercial distribution, specialty pharmacy operations, S&OP processes, strategic long-term planning and key partner relationships (NeoPharmed Gentili, Torii/Orphan Pacific, Kaken, etc.) Collaborates closely with Logistics function to ensure all product movements are executed using qualified vendors, validated lanes and utilize intermediate warehouses/free trade zones (FTZ) to ensure compliant and optimized shipping/storage. Collaborates with Quality, Regulatory, Finance and Pharmaceutical Sciences to ensure proper vendor management and on-time movement of product. Manages overall S&OP and Capacity Planning processes interfacing with Commercial, GMS, Finance, Pharmaceutical Science and Global Partners (NG, Kaken, OP/Torii, etc.) to ensure accurate planning, inventory management and timely supply. Manages overall relationship with assigned Partners/Suppliers/3PL's and related internal BioCryst resources to deliver key

Sr. Advanced Analytics Manager US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The Sr. Advanced Analytics Manager will be responsible for managing analytics activities to support a data-driven culture within BioCryst by developing and applying analytic methodologies to deepen insights and inform commercial business decisions. The Sr. Advanced Analytics Manager will be a key member of teams responsible for the support of BioCryst's first commercial product launch of ORLADEYO for the treatment of hereditary angioedema, in addition to other products in the BioCryst rare disease pipeline. ESSENTIAL DUTIES & RESPONSIBILITIES: Advanced Analytics Partner with Advanced Analytics, Market Insights and Strategic Operations to integrate data, analytical methods, and insights across the organization to help inform strategic choices and measure performance. Lead the implementation and execution of commercial sales incentive plans to drive sales performance and to ensure alignment

Assoc. Director, IT Business Partner - G&A US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: BioCryst is a fast-growing pharmaceutical company seeking an experienced Associate Director, IT Business Partner to build and mature business partnerships across G&A functions, including Human Resources, Legal, Finance, Procurement, Supply Chain, Corp Comm and IT. This role serves as a strategic IT business partner and technology advisor, responsible for understanding functional goals, shaping the technology roadmap, and enabling system and process improvements across these areas. The Associate Director leads initiatives involving business analysis, project management, solution design, vendor collaboration, and technology enablement. This role ensures high satisfaction with IT systems and services, with emphasis on platforms such as Oracle Cloud Fusion, Workday, OIC, Contract Management system and finance applications, along with other G&A enablement systems. ESSENTIAL DUTIES & RESPONSIBILITIES: Serve as the

Assoc. Director, AI Enablement & IT Training 2 Locations COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. ESSENTIAL DUTIES & RESPONSIBILITIES: This role combines AI operational enablement, cross department collaboration, and IT training ownership. It is responsible for ensuring that AI and IT tools are not only deployed but actively used and integrated into how BioCryst teams work every day. Own the day today operational enablement of Microsoft 365 Copilot across the enterprise Configure, test, enable, and maintain Copilot features, settings, and options within the Microsoft ecosystem Ensure Copilot remains functional, secure, and usable as Microsoft introduces updates and new capabilities Partner with IT security, infrastructure, applications, and service teams to align AI enablement with operational standards Translate AI capabilities into practical, repeatable use cases that improve employee productivity Support responsible, compliant, and scalable use of AI technologies Work directly with

Sr. Manager, Regulatory Affairs US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The Sr. Manager, Regulatory Affairs at BioCryst Pharmaceuticals (BioCryst) will work closely with product development core teams and subteams in setting company goals and work closely with these groups in meeting company goals. This position will be responsible for ensuring efficient and productive regulatory submissions for BioCryst, as well as assisting and collaborating in strategic drug development program implementation. The position will work to develop and implement key new values and added initiatives focused on the coordination of the company's regulatory program and product development missions. ESSENTIAL DUTIES & RESPONSIBILITIES: Manage and support the preparation of US regulatory submissions including INDs and NDA/BLAs as well as regulatory submissions outside the US on assigned projects. Support regulatory strategies for assigned projects via researching regulations and guidelines

Business Operations Manager (R&D) US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The R&D Business Operations Manager will be the lead support function for Chief R&D officer and also provide support to his Leadership Team as needed. We are seeking a high-caliber professional to support our R&D leadership team by bridging the gap between administrative and operational excellence and strategic communication. This role is pivotal for managing the logistics of an R&D leadership team in a growing biotech firm while helping shape the narrative for our global team. The ideal candidate will be highly organized, agile, adaptable with good communication skills and a motivated team player to support the R&D leadership. In addition, it is preferred that the candidate will be physically located in the Boston, MA, or Durham, NC areas. ESSENTIAL DUTIES & RESPONSIBILITIES: Key Responsibilities

Director, Market Access & Policy - Canada 4 Locations COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. ESSENTIAL DUTIES & RESPONSIBILITIES: Develop and implement national and provincial market access and stakeholder engagement strategies to ensure optimal policy conditions and reimbursement for current and future BioCryst products. Lead development and submission of HTA dossiers to bodies such as CDA and INESSS. Effectively navigate the pCPA environment; lead negotiations with pCPA and provinces to secure PLAs. Lead development of all provincial healthcare payer and private payer reimbursement files; lead negotiations of PLAs with public and private payers. Support the development and implementation of annual plans for public and private payer customers in Canada. Manage all public and private payer and policy related issues. Lead all required annual reporting, incl. PMPRB, provincial/territorial payers, private payers. Ensure compliance with PMPRB (Patented Medicine Prices Review Board)

Director, Global Regulatory CMC US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The Director, Global Regulatory CMC will work closely with project teams and CMC Leadership in setting and meeting company goals as they relate to CMC matters. This position will be responsible for ensuring efficient and productive strategic and operational regulatory CMC support for BioCryst development programs. The position will work to develop and implement key new values and added initiatives focused on the coordination of the company's regulatory CMC program with the Clinical, Nonclinical, Regulatory, and QA groups. This position will be responsible for development and implementation of a Global Regulatory CMC plan, addressing research and product development needs, as well as the integration of the global regulatory strategic plan into the research, and product developmental missions. ESSENTIAL DUTIES & RESPONSIBILITIES: Manages all global regulatory

Director, Quality Control US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The Director, Quality Control (QC) is responsible for providing strategic and operational quality oversight of all Quality Control (QC) activities supporting the development, manufacture, testing, release, and lifecycle management of small molecule, large molecule/biologic, and combination products. The Director, Quality Control provides technical leadership and scientific decision‑making for analytical control strategies, method performance, reference standards, specifications, and laboratory investigations, serving as a recognized technical authority for QC‑related matters across the product lifecycle.This role ensures QC activities are executed in compliance with global GxP regulations and internal Quality Systems. The Director serves as the primary Quality authority for QC compliance, analytical control strategy, investigation oversight, stability programs, reference standards, and test method governance, and partners closely with Analytical Development to ensure effective method design, lifecycle transfer, performance

VP, MS&T US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram. JOB SUMMARY: The Vice President, Manufacturing Sciences & Technology (MS&T) is a critical, enterprise-level leadership role reporting to the Senior Vice President, Technical Development & Manufacturing (or Global Supply Chain). The Vice President leads the MS&T function in support of both biologics (recombinant proteins, monoclonal antibodies, and drug delivery devices) and small molecule programs, overseeing the entire lifecycle from late-stage development through commercial launch and lifecycle management. This position is accountable for developing and executing strategies that ensure robust, compliant, and scalable manufacturing processes, and for scaling the MS&T organization to support rapid pipeline and commercial growth. The role has high visibility and strategic influence across Technical Operations, Supply & Manufacturing, Regulatory Affairs, Pharmaceutical Sciences, and Quality, managing a team of technical leaders and interfacing with internal and external

Medical Science Liaison - Southeast region US_North Carolina_Remote COMPANY: At BioCryst, we share a deep commitment to improving the lives of people living with complement-mediated and other rare diseases. For over three decades we've been guided by our passion for not settling for “ordinary” in our quest to develop novel medicines. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and protein therapeutics, led by the efforts of our team of expert scientists in our Discovery Center of Excellence in Birmingham, Alabama. Our global headquarters is in Durham, North Carolina and our employees span the globe across sites in multiple countries. We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at www.biocryst.com or follow us on LinkedIn and Instagram . JOB SUMMARY: BioCryst Pharmaceuticals is seeking an experienced Medical Science Liaison (MSL) to join our US Medical Affairs team. As a field-based MSL you will be a true scientific, medical expert and an extension of BioCryst Medical Affairs. You will build and facilitate strategic peer-to-peer relationships with key Health Care Providers (HCP) in the assigned region. You will be providing credible and unbiased scientific information, identifying and executing the strategic Medical Affairs Plan and supporting home office medical activities. Strong emphasis on collaboration w/ cross-functional colleagues as appropriate. Candidates must reside in a state within the Southeast region: FL, AL, GA, MS, or Puerto Rico.

Director, US Value and Access Strategy, Enzyme Therapies Director, US Value and Access Strategy, Enzyme Therapies

Associate Director, Bioanalytical Development New York, NY; Boston, MA About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others. You can read more at the following links: - Our Vision for AI in Pharma - Our Current Drug Portfolio - Our Technology & Platform At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently. About the Position The Associate Director, Bioanalytical will lead bioanalytical strategy and delivery for assigned programs, working across nonclinical and clinical

Director, Business Development - Search & Evaluation Boston, MA About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidate drugs than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of new medicines that can reach patients, Formation Bio, founded in 2016 as TrialSpark Inc., has built technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech, including a16z, Sequoia, Sanofi, Thrive Capital, John Doerr, Spark Capital, SV Angel Growth, and others. You can read more at the following links: - Our Vision for AI in Pharma - Our Current Drug Portfolio - Our Technology & Platform At Formation Bio, our values are the driving force behind our mission to revolutionize the pharma industry. Every team and individual at the company shares these same values, and every team and individual plays a key part in our mission to bring new treatments to patients faster and more efficiently. About the Position The Director of Business Development, Strategic Sourcing, will play a key role in identifying, evaluating, and managing early-stage

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

Director, Patient Marketing 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 Director, Patient Marketing, will be instrumental in crafting and implementing strategies and tactics tailored to the rare disease community. Your responsibilities will include spearheading a range of initiatives, from near-term execution to developing new capabilities for mid-to-long-term brand success. This encompasses managing educational initiatives, cultivating relationships with key opinion leaders, and ensuring all marketing initiatives for patients and healthcare professionals adhere to company compliance standards. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop comprehensive patient-centric strategies across multiple disease states including understanding the patient journey, identifying unmet needs, developing innovative solutions, and executing programs to meet those needs. Lead patient ambassador programs to include

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