13 Global Affairs Jobs in Westborough, MA
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Global Head, Infection Prevention Olympus Corporation of the Americas - Westborough, MA, US , staff meetings, and global meetings. Collaborate with the Chief Medical Safety Officer, Chief Medical Officer, and other senior leaders within Medical and Scientific Affairs to share best practices 3 days ago
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Senior Manager, Business Development Quality Assurance Olympus Corporation of the Americas - Westborough, MA, US . Integrate the target site into the Olympus quality culture and ensure cohesive transition into full integration. Stay up to date on the latest global regulations. Collaborate closely with the Quality More than 30 days ago
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Senior Director/Director, Global Regulatory Affairs Lead Corbus Pharmaceuticals - Norwood, MA, United States Collaborate with the leadership team to develop Regulatory Strategy as part of an integrated development plan for each Corbus asset... 4 days ago
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Regulatory Project Manager (Part time) Tandym Group - Woburn, MA, United States the execution of regulatory strategies within the Global Regulatory Affairs function with specific focus on regulatory filing activities, project management tools, and communication. **This job is a remote 6 days ago
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Principal Regulatory Affairs Specialist Boston Scientific - Marlborough, MA, US Recruiter: Spencer Gregory Hale Principal Regulatory Affairs Specialist About the role: Magellan is a global business transformation program accompanying a move of our ERP system from SAP ECC to S4 15 days ago
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Late Clinical Development, Medical Director AstraZeneca - Waltham, Massachusetts, USA protocol and its governance approval. Supports or leads interactions with global medical affairs, marketing companies, commercial, and regulatory functions in collaboration with GCH/GCPL to ensure cross 4 days ago
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Regulatory Affairs Director, Oncology AstraZeneca - Waltham, Massachusetts, USA of the regulatory strategy document and target product labeling. Own the negotiations with health authorities and initiate and deliver key regulatory documents. Plan and construct the global dossier and core 7 days ago
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Medical Writer Novo Nordisk - Lexington, MA with global and local cross-functional study teams, including personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs, Global Safety, Data Management 23 days ago
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Director/Senior Manager, Medical Affairs ConvaTec - Lexington, Massachusetts, USA , such as the identification of unmet needs, planning of evidence generation strategies, designing clinical studies and retrospective analyses, and generation of publications. You will have close liaison with Clinical Affairs 18 days ago
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Senior Medical Director Novo Nordisk - Lexington, MA , , Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal TRU and Novo Nordisk global development leadership, and external stakeholders including KOLs 16 days ago
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- Cambridge, MA (19)
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