107 Drug Regulatory Affairs Jobs - page 2
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Senior Director/Director, Global Regulatory Affairs Lead (remote) Corbus Pharmaceuticals - Norwood, MA, United States in Regulatory Affairs Experience in all types of regulatory submissions including but not limited to INDs, NDAs, MAA, Type A-D Meetings with FDA, Scientific Advice Consultations with the CHMP of EMA and MHRA, MAA 5 days ago
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Regulatory Affairs Senior Manager - Vascular (on-site) Abbott Laboratories - Santa Clara, California , balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. This Regulatory Affairs Senior Manager position is an onsite opportunity working out of our Santa 2 days ago
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Regulatory Affairs Specialist Highridge Medical - Westminster, CO, United States area. Ability to build relationships between Regulatory Affairs and other areas of the organization; ability to communicate effectively at all levels. Knowledge of FDA, EU, and other regulatory body 7 days ago
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Director, CMC Regulatory Affairs Bayside Solutions - , CA, United States related field is preferred. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC 8 days ago
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Senior Regulatory Affairs Specialist - Vascular (on-site) Abbott Laboratories - Santa Clara, California , balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an on-site opportunity working out 2 days ago
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Associate Director, Clinical Study Manager, Rare Disease, Oncology Connect Life Sciences - , CA, United States for approval. This role establishes and maintains effective communication and collaboration with functional area peers including Drug Safety, Clinical Quality Assurance, Regulatory Affairs, Clinical Development 8 days ago
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Scientific Program Manager - HESI Health and Environmental Sciences Institute (HESI) - Washington, DC, United States , pathology, chemistry, environmental health, or related life sciences and a minimum of 3 years of experience in project management, drug or chemical safety evaluation, scientific consulting, and/or regulatory 8 days ago
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Senior Manager, Medical Affairs Quality ( On-site, IL based) North Chicago, IL for providing independent quality oversight of GxP activities executed by AbbVie's Medical Affairs enterprise, including but not limited to non-interventional studies, medical information and other regulatory 6 days ago
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Director, Regulatory Affairs Strategy SciPro - , NJ, United States for specific assets within Oncology. The position will report directly into the VP of Regulatory Affairs. The company is growing exponentially with a focus in drug development within the oncology space 8 days ago
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Medical Officer (TB Clinical Research) - NIH Kelly - Rockville, MD, United States particularly the safety of the drug in question (5) Evaluate annual IND annual reports for medical safety and report findings to Regulatory Affairs Branch (RAB). (6) Provide medical expertise in protocol follow 19 days ago
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