- Merck (Rahway, NJ)
- **Job Description** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy ... global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. + Develops worldwide… more
- Ascendis Pharma (Princeton, NJ)
- …committed to working together as one team to achieve extraordinary results. The Associate Director Regulatory Affairs , Advertising and Promotion will be an ... promotion of prescription drug and biologic products. The Associate Director Regulatory Affairs , Advertising and...and/or disease education communications + Serve as the company's regulatory liaison to the FDA's Advertising and… more
- Sumitomo Pharma (Trenton, NJ)
- …seeking a dynamic, highly motivated, and experienced individual for the position of **Associate Director , Regulatory Affairs ** . The Associate Director ... is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will...the GRL, may lead regional Health Authority meetings and liaison with local Health Authority and company governance boards… more
- Sumitomo Pharma (Trenton, NJ)
- …are currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Director Regulatory Affairs ** . The Director is part ... of the Global Regulatory Affairs (GRA) team based in the US. He/she will...Health Authorities + Leads the regional health authority meetings, liaison with local Health Authority, + Document owner of… more
- Bristol Myers Squibb (Princeton, NJ)
- …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... will meet global regulatory requirements by soliciting and integrating regional regulatory strategy liaison input. In collaboration with the Global … more
- Merck (Rahway, NJ)
- **Job Description** **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and ... and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. **Key Functions**… more
- AbbVie (Florham Park, NJ)
- …statistics, regulatory , etc.) as they relate to on-going medical affairs projects. + Experience in Neuroscience/Psychiatry preferred. + May assist as consultant ... be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational input into core… more
- City National Bank (New York, NY)
- * DIRECTOR BUSINESS AFFAIRS * *WHAT IS THE OPPORTUNITY?* This position provides overall management of significant City National Rochdale (CNR) projects on a ... the firm's activities ensuring that legal issues, contracts, disputes, and complex regulatory and operational risk activities are conducted within the due diligence… more
- Lilly (New York, NY)
- …wage for this position is $145,500 - $213,400 **Purpose:** The Health Outcomes Liaison (HOL) team serves as the medical and health economic and outcomes research ... + Stay abreast of emerging science, environmental trends, healthcare policy, and regulatory actions relevant to US population-based decision-makers + Serve as a… more
- Ascendis Pharma (Princeton, NJ)
- …projects to both internal and external audiences within legal, compliance and regulatory guidelines. + Represent Ascendis Medical Affairs internally and ... Medical Director Do you want to be part of building...well functional projects as part of the US Medical Affairs Team. They will be accountable and help the Head… 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 ... to make a difference? The Position The International Medical Director serves as a subject matter expert for our...Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive… 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 ... make a difference? The Position The Senior International Medical Director serves as a subject matter expert for our...Non-Clinical Research, Medical Writing, Program Management, Product Supply and Regulatory Affairs teams to deliver and drive… more
- City of New York (New York, NY)
- …(NOVA) program located at the DHS intake center and the Domestic Violence Liaison Unit, which provides domestic violence counseling and intervention at Job Centers. ... Abuse Prevention Program (RAPP). Under administrative direction of the Senior Director of Administration Planning Operations and Emergency Support Services, the … more
- Sanofi Group (Bridgewater, NJ)
- **Job Title:** US Medical Director , Mainline Vaccines **Location** : Bridgewater, NJ / Morristown, NJ **About the Job** The North American Medical Team at Sanofi is ... millions of patients around the world. **Main Responsibilities:** The US Medical Director , Mainline Vaccines, will contribute to development and execution of the… more
- City of New York (New York, NY)
- …and acting as a liaison with various DDC groups, DOT, DEP, and regulatory agencies like the NYS Department of Environmental Conservation and the US Army Corps of ... of Design and Construction's Division of Infrastructure is in search of a Director for the Bluebelt and Wetland team. Under the Assistant Commissioner's direction,… more
- Cline Davis & Mann (New York, NY)
- …and assist the "onboarding" process for new team members. The VP, Medical Director must demonstrate clinical and technical knowledge of medicine across a broad range ... and strategic relevance. In addition,theywill develop relationships with leading marketing, regulatory , medical, and clinical personnel at the client as well as… more
- Mallinckrodt Pharmaceuticals (Bridgewater, NJ)
- …and trial design specific to drug delivery and feasibility, acting as a liaison between potential investigators and Medical Affairs , and supporting data and ... pharmaceuticals, marketing, sales, research and development, strategy and portfolio management, regulatory , technical services, and medical affairs team members.… more
- Research Foundation CUNY (New York, NY)
- …Support Office, RCMI editing core, Internal Advisory Board, and any relevant regulatory affairs committees for the eventual submission of final proposals ... Investigators (MPIs) and reporting directly to the Investigator Development Core (IDC) director , the Project Manager (PM) supports the coordination of the IDC Pilot… more