- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... with talented and dedicated colleagues while developing and expanding your career.The Senior Director ( Senior Principal Scientist ) has primary responsibility… more
- Merck & Co. (Rahway, NJ)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... dedicated colleagues while developing and expanding your career.-- Director (Principal Scientist ) has primary responsibility for the planning and directing of… more
- Merck & Co. (Rahway, NJ)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist )...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations, ... The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …including working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
- 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...CMC Biologics (R5)** Under general supervision of an Executive Director/ Senior Director, the Principal Scientist /Director is… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... talented and dedicated colleagues while developing and expanding your career. The Senior Director ( Senior Principal Scientist ) has primary responsibility… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …with cross functional teams and various departments to include Marketing, Medical Affairs , Regulatory Affairs , Supply Chain Technical Operations, ... The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, Manufacturing, and Controls) activities of the portfolio small… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …including working with contract manufacturing organizations CMO.** This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub ... applications/supplements & variations (eg, NDA, BLA, MAA). This position authors regulatory documents where necessary with supervision. This position conducts … more
- Pfizer (New York, NY)
- …leaders and projects team members, including research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational oncology, ... **ROLE SUMMARY:** The overall role of the Oncology Early Stage Clinical Scientist (ESCS) is to lead and coordinate the development of multiple studies for novel… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... dedicated colleagues while developing and expanding your career. Director (Principal Scientist ) has primary responsibility for the planning and directing of clinical… more
- City of New York (New York, NY)
- …where they are from or where they live. Position Summary: BHHS's Policy and External Affairs Program seeks a Senior Policy Advisor to lead its health systems ... and Treatment, HIV Epidemiology, HIV Prevention, Policy and External Affairs , Racial Equity and Social Justice Initiatives, STI, and...STI, and viral hepatitis policy advocacy more broadly. The Senior Policy Advisor will report to the Director of… 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Senior Medical Director, Clinical Sciences, Hematology provides clinical leadership and is responsible for all clinical deliverables within the assigned section ... with the Clinical Development Plans (CDP); clinical components of regulatory documents/registration dossier and brand related medical information, clinical… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …looks like:** + Partners with the CDSL Managers, the Formulation Development Group (FDG), Regulatory Sciences (RS)/ Affairs (RA), as well as members of the ... The Senior Manager, Pharmacy Support Lead (PSL) is responsible...Study Lead (CSL), Study Medical Director (SMD) and Clinical Scientist (CS), Quality Management Lead (QML **).** + Provides… more
