20 International Clinical Research Jobs in Lexington, MA
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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 13 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 15 days ago
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Senior Clinical Project Manager / Senior Clinical Study Manager ConvaTec - Lexington, Massachusetts, USA clinical studies. • Advanced Knowledge of the federal regulations governing research and the standards defining Good Clinical Practices (GCPs). • Fluent verbal and written English essential. • Multilingual 15 days ago
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Medical Director Novo Nordisk - Lexington, MA with SOPs, ICH, GCP and other national and international regulatory requirements Work with, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams 17 days ago
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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 14 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 11 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 4 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 11 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 23 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 11 days ago
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