- Merck (Rahway, NJ)
- …product withdrawal. + Support new technology development. + Demonstrate an understanding of regulatory affairs and applies this understanding to the benefit of ... **Job Description** ** Principal Scientist / Director, GLOBAL REGULATORY ...CMC Biologics (R5)** Under general supervision of an Executive Director/ Senior Director, the Principal Scientist /Director is… more
- Merck (Rahway, NJ)
- …talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Senior Principal Scientist) has primary responsibility ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... and dedicated colleagues while developing and expanding your career. Director ( Principal Scientist) has primary responsibility for the planning and directing of… more
- Insight Global (New York, NY)
- Job Description Insight Global is looking for a Senior Regulatory Project Manager to join one of our financial clients in NYC. This individual will be reporting ... be responsible for delivering on complex projects within the Regulatory Affairs Program portfolio. Day to day...Day to day responsibilities will also include being the principal liaison between the business, IT, and senior… more
- Merck (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The ** Senior Clinical Director (Sr. Principal Scientist)**...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior … more
- Edwards Lifesciences (Newark, NJ)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and … more
- City of New York (New York, NY)
- …(OQA&FI) / The Process Evaluation Review Team (PERT) is recruiting for (2) one Principal Administrative Associates III, to function as Senior Case Reviewers who ... of Quality Assurance & Fiscal Integrity ensures the integrity, efficiency, and regulatory compliance of agency operations, advising programs of potential risks and… more
- Edwards Lifesciences (Newark, NJ)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and … more
- Hackensack Meridian Health (Edison, NJ)
- …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the ... at Hackensack Meridian _Health_ includes: + Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory … more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Clinical Director ( Principal Scientist) has primary responsibility for planning and directing clinical research activities involving… more