31 Regulatory Affairs Cro Jobs - page 2
-
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 16 days ago
-
Associate Director / Director of Bioanalysis Larimar Therapeutics - Bala Cynwyd , Pennsylvania 19004 , United States -clinical & clinical operations) and regulatory affairs to support drug discovery and development programs. Author/contribute to bioanalytical reports and ensure accurate records of experimental procedures 2 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 14 days ago
-
GPV Submission Specialist GForce Life Sciences - Princeton, NJ, United States , biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Monitor, Regulatory Affairs, or Quality Assurance Required Skills 15 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 8 days ago
-
GPV Case Management Product Specialist GForce Life Sciences - Trenton, NJ, United States , biotechnology, or CRO industry, partly in related areas such as Medical Affairs, Clinical Data Entry and Clinical Data Management, Clinical Monitor, Regulatory Affairs, or Quality Assurance Required Skills 15 days ago
-
Medical Director of Ophthalmology Beacon Hill - , MA, United States as the primary sponsor contact for clinical issues relating to assigned clinical trials. Providing clinical and medical support to the CRO, as well as regulatory, safety and other functions, for assigned clinical 14 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 17 days ago
-
Senior Manager/Associate Director, Clinical Project Manager PepGen - Boston, MA, United States safety. Responsibilities Lead the cross functional study team for the EDODM1 Phase 1 study, including clinical monitors, data management, biostatistics, medical writing, safety, regulatory affairs 21 days ago
-
VP Clinical Operations i-Pharm Consulting - Boston, MA, United States with cross-functional teams, including Clinical Development, Regulatory Affairs, Quality Assurance, and other departments, to ensure seamless integration and coordination of clinical activities. Establish 22 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)
- See more