- Merck (Rahway, NJ)
- **Job Description** We are seeking a Senior Director (Sr. Principal Scientist ) Global Regulatory Affairs Liaison with a visionary, growth-oriented ... priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and implementation… more
- Merck (Rahway, NJ)
- **Job Description** We are seeking a Director (Principal Scientist ), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... pipeline and drive our strategic priorities. The Director, Principal Scientist | Regulatory Affairs Liaison...+ Reports to Associate Vice President, Executive Director, or Senior Director in the General Medicine Therapeutic Area. +… more
- Haleon (Warren, NJ)
- …that's uniquely ours. Care to join us. It isn't a question. The ** Senior Scientist -Allergy, Medical Devices &** **NRT** will provide medical/scientific guidance ... Sciences or related field. + 2+ years of experience in Medical Affairs , R&D, Regulatory Affairs within the consumer healthcare or pharmaceutical industry. +… more
- Merck (Rahway, NJ)
- …Description of Position-** This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). ... **Job Description** **Position Title** -Director/ Principal Scientist , Regulatory Compliance **Department** - Device...final guidance and standards. + Provide strategic advice to senior management on CMC regulatory matters based… 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)
- …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)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… 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
- Novo Nordisk (Plainsboro, NJ)
- …the Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and ... with, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive the timely… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Senior Medical Director, Clinical Development, Oncology will function as clinical leader of a section of a clinical program (eg, an indication, a new ... also lead multi-disciplinary teams charged with guiding clinical development and subsequent regulatory submissions and may directly lead Medical Directors. As a … more
- Novo Nordisk (Plainsboro, NJ)
- …Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs , Data Management, Biostatistics, Non-clinical, Medical ... safety surveillance sub-function within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and Senior Global Safety… 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