Sr. Medical Director, Clinical Development (Psychiatry) AlkermesSr. Medical Director, Clinical Development (Psychiatry)Waltham, MARemote$340,000–$360,000 / yearThis position will work cross-functionally to ensure projects are coordinated with partners from multiple departments within Alkermes including regulatory, preclinical research, clinical pharmacology, translational medicine, toxicology, CMC, new product planning, project management, patient engagement, health economics, legal, finance, medical affairs and commercial. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
Executive Medical Director, Clinical Development (Psychiatry) AlkermesExecutive Medical Director, Clinical Development (Psychiatry)Waltham, MARemote$360,000–$390,000 / yearThis position will work cross-functionally to ensure projects are coordinated with partners from multiple departments within Alkermes including regulatory, preclinical research, clinical pharmacology, translational medicine, toxicology, CMC, new product planning, project management, patient engagement, health economics, legal, finance, medical affairs and commercial. Additionally, the Executive Medical Director will participate in internal strategy regarding future therapeutic priorities and interact externally with key global regulatory authorities, industry and scientific organizations, as well as external key thought leaders.
Medical Director, Clinical Development (Neurology) AlkermesMedical Director, Clinical Development (Neurology)Waltham, MARemote$286,000–$310,000 / yearThis position will work cross-functionally to ensure projects are coordinated with partners from multiple departments within Alkermes including regulatory, preclinical research, clinical pharmacology, translational medicine, toxicology, CMC, new product planning, project management, patient engagement, health economics, legal, finance, medical affairs and commercial. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts' Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine.
GCP Operational Quality Senior Manager Vertex Pharmaceuticals IncGCP Operational Quality Senior ManagerBoston, MARemote$137,800–$206,800 / yearGeneral Summary: The Senior Manager, Clinical Study Quality Lead provides study-level quality oversight for assigned clinical trials to help ensure they are conducted in compliance with Good Clinical Practice (GCP), applicable global regulations, study protocols, and Vertex procedures. This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support, compliance trend analysis, and inspection readiness.
TMF Specialist Actalent IncTMF SpecialistNorth Billerica, MARemote$42–$58 / hourYou will work closely with cross-functional partners in Clinical Operations, Quality Assurance, Regulatory Affairs, Medical Writing, Data Management, Safety, CROs, and external vendors, using Veeva Vault eTMF and Veeva Clinical platforms as core systems for TMF management. This role ensures that approximately 45,000 TMF documents from non-active studies are accurately scanned, filed, indexed, classified, and maintained in alignment with internal procedures, the TMF Reference Model, study-specific TMF plans, and applicable regulatory requirements.
Director, Market Access and Reimbursement Veranex IncDirector, Market Access and ReimbursementBoston, MARemoteAs the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting. The Director, Market Access and Reimbursement will be responsible for leading the successful execution of client engagements through strategic planning, comprehensive project management, external vendor oversight, and the development and delivery of high-quality client solutions.