Latest Drug Development jobs in Raritan, NJ - JobisJob United States Mobile

137 Drug Development Jobs in Raritan, NJ

Associate Director, Clinical Sciences - Ophthalmology Johnson & Johnson - Raritan, NJ data review, including medical data review, coding, in conjunction with other clinical team members. OTHER RESPONSIBILITIES / DETAILED DUTIES: Assists Regulatory Affairs in the development of drug USD 135,000.00 - 232,300.00 per year 11 days ago
Medical Director, Bladder - Global Medical Affairs Oncology Johnson & Johnson - Raritan, NJ research and its application to drug development is required. Experience specifically in bladder, is highly desired, with experience working with experts in the medical community. Good oral, written USD 187,000.00 - 322,000.00 per year 14 days ago
Senior Regulatory Affairs Associate Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States in drug development from early stage development through final formulation, ensuring compliance with principles of Quality-by-Design, cGMP, and FDA rules and regulations Support new product launches 5 days ago
Senior Director, Global Regulatory Leader, CAR-T Therapy Johnson & Johnson - Raritan, NJ sciences or technical discipline is required An advanced degree in the biological sciences is preferred (e.g., M.S., Ph.D., M.D.) Experience and Skills: Required: A minimum of 15 years in drug development USD 187,000.00 - 322,000.00 per year 24 days ago
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Endocrine Clinical Sales Specialist - Philadelphia Ascendis Pharma - New Brunswick, NJ, United States , and Passion, they use their TransCon® drug development platform to fulfill their mission of developing new and potentially best-in-class therapies to address unmet medical needs. Their culture fosters a place 9 days ago
Senior Manager Regulatory Affairs Gan & Lee Pharmaceuticals - Bridgewater, NJ, United States in a scientific or related discipline, 5+ years of pharmaceutical industrial experience, at least 3 years of regulatory CMC experience with US product development. • Deep knowledge of US and EU regulations 29 days ago
Director, Clinical Pharmacology Insmed Incorporated - Bridgewater, New Jersey for clinical and non-clinical studies Apply model-based drug development strategy to support clinical dose and dosing regimen selection, facilitate clinical study design and support regulatory submissions Author 10 days ago
Analytical Chemist Ivory Systems - Hopewell, NJ, United States methods, and reports. Perform routine analytical tests (e.g., SEC, CE, ICIEF, Protein A) to support the upstream and downstream process development. • Support the development and transfer of analytical 6 days ago
Analytical Development Analyst Randstad Life Sciences US - Hopewell, NJ, United States process development. Support the development and transfer of analytical methods of biologics drugs (including monoclonal antibodies, bispecific antibodies, ADC). Understand CMC process of biologics drugs 6 days ago
Director Toxicology Insmed Incorporated - Bridgewater, New Jersey record of successfully leading toxicology programs through various stages of drug development. Experience in toxicology on biologics, oligonucleotides, and/or gene therapies is a plus. Advanced knowledge 15 days ago

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