20 International Clinical Research Jobs in Boston, MA - page 2
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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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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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VP of Global Clinical Operations Jobot - Boston, MA stakeholders, including investigators, medical professionals, executives and regulatory authorities, to ensure the highest standards of clinical research are met. Responsibilities: Provide strategic leadership $330,000 - $360,000/Year 21 days ago
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Senior Clinical Data Manager AL Solutions - Cambridge, Massachusetts activities. Requirements: Bachelor’s degree in a related field & 5 years of relevant experience required; at least 3 years experience in clinical data management in a clinical research setting also required. 2 30 days ago
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usa-scientist iii (scientific)- first shift Randstad - cambridge, massachusetts (remote) /retina experience is required A minimum of 3 years of clinical research and clinical drug development experience within the ophthalmology/retina pharmaceutical industry or CRO is required Knowledge in ICH $85 - $88.26 per hour 26 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 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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USA Scientist III Scientific Adecco Medical & Science - Cambridge, MA of clinical research and clinical drug development experience within the ophthalmology/retina pharmaceutical industry or CRO is required Knowledge in ICH - GCP (Good Clinical Practices) (International $85.00 - $86.43/Hour 25 days ago
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