20 International Clinical Research Jobs in Burlington, MA
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Executive Director, Medical Writing MapLight Therapeutics, Inc. - Burlington, MA, United States /CTAs, NDA/BLA/MAAs Working knowledge of drug development, clinical research, study design, biostatistics, regulatory, and medical terminology Advanced knowledge of US and international regulations 13 days ago
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Clinical Scientist (Part-Time) 2026161 Stratacuity: Proven Scientific Placement - Cambridge, MA, United States Job Requirements: Bachelor's or master's degree in life sciences is required, while a PharmD or PhD is preferred. Two 2+ years’ experience in Clinical Research is necessary, with specific experience in executing 10 days ago
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Clinical Trial Assistant Scholar Rock - Cambridge, Massachusetts %)RequirementsBachelor’s Degree PreferredExperience in a CRO, Sponsor or clinical research administration function, including hands on experience relating to the essential documentation of a clinical trial. Experience 3 days ago
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Regulatory Affairs Manager Genabio Diagnostics - Bedford, MA, United States and external government product audits by FDA and other inspection agencies as needed and support the implementation of clinical research projects and support clinical sites management through all phases 22 days ago
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Clinical Trial Manager EPM Scientific - Boston, MA, United States and company objectives. This role will involve close collaboration with cross-functional teams, including clinical research, regulatory affairs, and data management. Key Responsibilities: Oversee the planning 10 days ago
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Vice President, Oncology Breast Therapeutic Area Medical Head , NMD at Pfizer Pfizer - Cambridge, Massachusetts Strategy, Clinical Development and Operations, Translational Oncology, US Medical Affairs, etc.), International Oncology Medical Affairs, Pfizer Research & Development (PRD) cross-TA global Medical platforms 10 days ago
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Senior Manager, Pharmacovigilance and Drug Safety ONO PHARMA USA - Cambridge, MA, United States in preparing SAEs, and authoring individual and aggregate safety documentation. Experience managing pharmacovigilance activities and building collaborative relationships with clinical research organizations 28 days ago
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Senior Medical Director Novo Nordisk - Lexington, MA of clinical trials Ensure compliance with SOPs, ICH, GCP and other national and international regulatory requirements Work with the VP Medical/Scientific Development, Clinical Operations, Non-Clinical Research 12 days ago
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Director/Senior Manager, Medical Affairs ConvaTec - Lexington, Massachusetts, USA and international standards and regulations for conduct of clinical research. • Demonstrated medical writing capabilities and experience in performing literature reviews. • A proven ability to deliver results 14 days ago
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Medical Science Liaison, Psychiatry - Northeast Lundbeck - Boston, Mass, US experience as an MSL within a pharmaceutical or biotech company Experience in various fields in CNS such as Psychiatry Experience in clinical practice, research, or teaching TRAVEL: Willingness/Ability 4 days ago
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