31 Regulatory Affairs Cro Jobs - page 3
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North American Regulatory Expert Medpace, Inc. - Cincinnati, Ohio Management, and Biostatistics. Qualifications : • PhD in Life Sciences or PharmD • 3+ years of regulatory affairs experience in a CRO or Pharmaceutical industry Medpace Overview : Medpace is a full-service 21 days ago
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Regulatory Operations Contractor Beacon Hill - Boston, MA, United States Recent Pharma/ CRO experience required Regulatory Operations Contractor Regulatory Affairs Location(Boston) Contract Term: Contract through EOY with possible extension Should have strong Word, PDF 24 days ago
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Senior Clinical Trial Manager BioPhase - , CA, United States Monitor, Regulatory Affairs, CRO, vendors and Investigators/site staff). Education/Experience Requirements: Bachelor’s in Life Sciences or equivalent. Graduate degree preferred. Therapeutic experience 27 days ago
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Vice President, Regulatory Strategy Medpace, Inc. - Cincinnati, Ohio Sciences, or other advanced degree. Minimum of 5 years of experience or equivalent of regulatory drug development. Expert knowledge of regulatory affairs within one or more therapeutic areas; Professional 21 days ago
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Clinical Program Manager Manpower San Diego - San Diego, CA, United States Executive Management, Product Development/R&D, Regulatory Affairs, Quality Assurance, and Operations as well as Clinical Research Organizations (CROs) to set operational direction and strategy for clinical 26 days ago
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Clinical Imaging Scientist - Late Development Oncology AstraZeneca - Mississauga, Canada development, clinical operations, data management, statistics, and regulatory affairs. CIS will liaise with both the internal clinical teams and external CROs where applicable. CIS will work closely 27 days ago
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Associate Director Pharmacovigilance Safety Scientist Spark Therapeutics - Philadelphia, PA, US to completion. Internal and External Contacts Internal Spark Contacts: Clinical Development Clinical Operation Regulatory Affairs Biometrics Corporate Quality Assurance Medical Affairs Cross-functional teams 29 days ago
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VP of Clinical Operations Theradaptive - Remote, United States and/or combination product clinical trials, quality assurance, and regulatory affairs within the biotech or pharmaceutical industry. * Strong leadership experience overseeing clinical operations teams, while managing More than 30 days ago
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Senior Director Oncology R&D Daiichi Sankyo, Inc. - Atlanta, GA ; Participates in creation of developmental and regulatory strategy in collaboration with Regulatory Affairs; Drafts clinical development plans, protocol profiles and sections of key submission documents; Point 14 days ago
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Clinical Research Technical Writer (remote) Arthrex - Naples, FL design information to prepare interim and final study reports Prepares clinical study documents and coordinates with additional collaborators including product management, statistician, regulatory affairs 3 days ago
Top locations
- Boston, MA (4)
- Santa Clara, CA (3)
- Indianapolis, IN (3)
- South San Francisco, CA (2)
- Cincinnati, OH (2)
- San Diego, CA (1)
- Brisbane, CA (1)
- New Haven, CT (1)
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