Latest Drug Regulatory Affairs jobs in Florham Park, NJ (page 2)

19 Drug Regulatory Affairs Jobs in Florham Park, NJ - page 2

Senior Principal Scientist, Clinical Research, Hematology/Lymphoma Merck - Rahway, NJ 07065 , the Senior Director may: Supervise the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs More than 30 days ago
Senior Director, Global Regulatory Leader, CAR-T Therapy Johnson and Johnson - Raritan, NJ years in drug development any of the following areas (e.g. Global Regulatory Affairs, R&D or health authority role) is required. * 10 years within the pharmaceutical/biotech industry is required, along 13 days ago
Program Manager, Clinical Database Services Merck - Rahway, NJ 07065 Team. Strong organizational, time management, and multi-project coordination skills Broad knowledge of Clinical Development and Regulatory Affairs requirements Ability to multi-task, work independently 18 days ago
Senior Medical Director, Oncology Asset Development Team Merck - Rahway, NJ 07065 the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage 22 days ago
Associate Director, Regulatory Strategy - Remote Agios Pharmaceuticals - Anywhere, New York, USA in Regulatory affairs strategy. Strong demonstration of knowledge of drug development, FDA, EMA and ICH guidelines and regulations Excellent organizational and communication skills, both written and verbal 26 days ago
Senior Clinical Director Merck - Rahway, NJ 07065 with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects. Assist the Executive Director in ensuring More than 30 days ago
Senior Principal Scientist, Thoracic Malignancies Merck - Rahway, NJ 07065 , the Director may: Supervise the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics 29 days ago
Clinical Supplies Manager SK Life Science, Inc. - Paramus, New Jersey experiences, etc. Manage and processing of CMC Team project invoices and internal project budget requests (ARIBA), and monitoring of project financial tracking. Assist and support Regulatory Affairs (RA 24 days ago
Director, Regulatory Affairs Companion Diagnostics Daiichi Sankyo, Inc. - Bernards, NJ experience including experience within Regulatory Affairs Understanding of scientific content and complexities and good knowledge of diagnostic development, including extensive experience of IDE submissions 3 days ago

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