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31 Regulatory Affairs Cro Jobs

Vice President of Clinical Operations Connecticut Innovations - New Haven, CT, United States , and regulatory submission. Collaborate closely with cross-functional program teams, including research and development, regulatory affairs, manufacturing, medical, and other relevant functions, to ensure effective 2 days ago
Associate Director, Clinical Science Maze Therapeutics - South San Francisco, CA, United States and budgets for clinical activities with overall company timelines and goals, in close coordination with project management, CMC, nonclinical development, regulatory affairs, and other stakeholders. Skills 2 days ago
Senior Manager, Clinical Supply Chain Agios Pharmaceuticals - Cambridge, Massachusetts, USA of drug supply materials. Work collaboratively with Clinical Operations, Quality Assurance, CMC and Regulatory Affairs to efficiently deliver clinical supplies as needed while ensuring compliance 2 days ago
Clinical Project Manager Meet - , TX, United States to protocol, budget, and timelines. Coordinate cross-functional teams, including Clinical Operations, Data Management, Regulatory Affairs, and Medical Affairs, to drive study milestones and deliverables 4 days ago
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Associate Director/Director, Regulatory Affairs 2025096 Stratacuity: Proven Scientific Placement - Boston, MA, United States or medical discipline and possess at least 5 years of experience in Regulatory Affairs within the pharmaceutical, biotechnology, CRO, or related industry. Additional Skills, licenses, or certifications 7 days ago
Clinical Data Manager Katalyst Healthcares & Life Sciences - South San Francisco, California Programming, Clinical Operations, Clinical Research, Quality Assurance, Global Patient Safety and Risk Management, and Regulatory Affairs; CROs, central and local laboratories, and other vendors. Establish 11 days ago
GCP Clinical Quality Assurance, Senior/Executive Director 89bio - , CA, United States , Clinical Development, CMC, Medical Affairs, Regulatory Affairs, CROs, CDMOs, Clinical Trial Sites, and laboratories. This role may have future leadership responsibilities building out a team and require 11 days ago
Drug Safety Specialist GForce Life Sciences - Waltham, MA, United States and investigator sites, interface with internal departments clinical operations, medical information, regulatory affairs, product development, quality assurance, biostatistics, data management, and legal 8 days ago
Program Manager 2-USD Mindlance - Auburn, Washington 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 11 days ago
Senior Director Regulatory Affairs SciPro - , NJ, United States the company's regulatory strategy having leadership over all regulatory activities Oversee product registration and submission Ensure compliance with FDA Work closely with CROs and manage relationships Provide 10 days ago

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