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Comprehensive understanding of related disciplines (biostatistics, regulatory affairs, pharmacology, toxicology, cell therapy manufacturing, clinical pharmacology, and pharmaceutical sciences.
$350,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provide operational expertise to internal and external teams (CMC, regulatory affairs, non-clinical, medical writing, data sciences, drug safety, CROs, consultants) to ensure that Clinical Development scientific and medical strategies are met.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Demonstrated knowledge of CMC development, CMC Regulatory Affairs, Quality Assurance and Control, cGMP and GLP requirements. As such, a successful candidate will possess experience and technical knowledge of CMC development, CMC Regulatory Affairs, Quality Assurance and Control, cGMP and GLP requirements.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are hiring in our Diagnostics Regulatory Affairs team here in San Diego, and are looking for a Senior Regulatory Affairs Specialist, IVD Product Lifecycle responsible for new product development, on-market, and international regulatory activities associated with US FDA, EU Notified Body, and other international regulatory agencies.
$173,900 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Support cross-functional launch teams, including marketing, sales, medical affairs, patient advocacy, regulatory, manufacturing, and supply chain, to ensure successful product launches. Strong understanding of drug development, regulatory, reimbursement requirements, and commercialization processes.
$299,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Vice President / Senior Vice President, Regulatory Affairs (VP/SVP) is the functional head leading regulatory activities on behalf of the Company. Serve as a member of the senior leadership team and provide regulatory affairs leadership and guidance and participate in leadership discussions on broader corporate considerations.
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The ideal candidate will have a strong background in biotech/pharma launch management from pre-regulatory submission to commercialization, exceptional leadership skills, and a proven track record of key contributions to successful product launches.
$299,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Senior Director, Regulatory Affairs will lead the Regulatory Affairs Strategy functions to support our clinical development programs (Phase 1, 2, 3) and planned future commercial launch.
$269,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Director/Senior Director, Regulatory Affairs Advertising and Promotion Boston, MA, San Diego, CA, or remote. The base range for a Director, Regulatory Affairs is $212,000 - $245,000 and Senior Director, Regulatory Affairs is $260,000 - $295,000 per year.
$295,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Pharmapace’s core mission is to deliver exceptional value to biotech/pharmaceutical companies by providing high-quality consulting and outsourcing services to support our customer’s clinical trials, regulatory submissions, medical affairs, safety surveillance, and outcomes research programs to help patients afflicted with a wide range of disease conditions.
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For more information, visit Position summary The Vice President / Senior Vice President, Regulatory Affairs (VP/SVP) is the functional head leading regulatory activities on behalf of the Company.
$350,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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We are in search of an accomplished and dynamic Senior Director of Regulatory Affairs to join our team. Minimum of 10 years of experience in Clinical Regulatory Affairs within drug development.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Reporting to the SVP, Regulatory Affairs, the Senior Manager or Associate Director of Regulatory Affairs will lead and participate in regulatory activities associated with IND/CTA preparations and maintenance to support new and ongoing development programs.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Shoreline Biosciences is seeking an experienced and talented Senior Director of Regulatory Affairs. 10+ years of Clinical Regulatory Affairs experience in drug development.
$307,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This role will interface with other Insulet departments (e.g. Sr. Management, Operations, and Information Technology, Engineering, New Business Development and Regulatory Affairs) as well as other external parties on issues related to product development, launched product support, and software used for automation of the quality system.
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regulatory affairs jobs Title: senior in San Diego, Beech-grove, Indiana
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