- Merck & Co. (Rahway, NJ)
- …preferred (engineering or scientific discipline, MBA)Knowledge of Global Regulatory Affairs and Clinical Safety organization, roles, and ... Job DescriptionThe Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global Regulatory Affairs … 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 ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. --Specifically, the Director may… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionTitle: Associate Principal Scientist/Associate Director , Outcomes ResearchRole SummaryUnder the guidance of a senior leader, an Associate Principal ... Scientist/Associate Director , has primary responsibility for planning/managing real world and...is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The… 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 ... analysis, regulatory reporting, and publication. - Specifically, the Senior Director may be responsible for Evaluating pre-clinical and translational work for… more
- Merck & Co. (Rahway, NJ)
- …partners including disease and alliance teams, research and development, medical affairs , regulatory affairs , market access, outcomes research, ... We are seeking a talented individual to join the team as Global Marketing Director to focus on expanding and growing our product, the first-and-only HIF2 inhibitor,… more
- Merck & Co. (Rahway, NJ)
- …and manage all communications across the vaccine portfolio and pipeline, including regulatory approvals, governing bodies, publications of scientific data and ... Job DescriptionThe Executive Director , Vaccines Communications is responsible for leading, developing and executing US and global communications strategies and… more
- Merck & Co. (Rahway, NJ)
- …a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing to ... clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards.-The Distinguished Scientist (Executive Director… 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 ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Clinical Director May Be… more
- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May… more
- Merck (Rahway, NJ)
- …(engineering or scientific discipline, MBA) + Knowledge of Global Regulatory Affairs and Clinical Safety organization, roles, and responsibilities. Current ... **Job Description** The Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global Regulatory … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across ... critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as...Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …for assigned cell and gene therapy portfolios. This role includes overseeing regulatory affairs staff, various outside contractors, supporting project teams and ... **In this role, a typical day might include:** + Direct activities of assigned Regulatory Affairs team with emphasis on global regulatory strategy and… more
- Bristol Myers Squibb (Madison, NJ)
- …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
- City of New York (New York, NY)
- …Mayor's Office of Community Mental Health (OCMH) is seeking a Deputy Executive Director , External Affairs who will head the multidisciplinary External Affairs ... Director of OCMH and will directly manage 4 staff members.The Deputy Executive Director , External Affairs will work closely with the Executive Director … more
- Teva Pharmaceuticals (Parsippany, NJ)
- …for media, investors, employees, and other audiences. The Director , Corporate Affairs - Brand Communications will translate the scientific significance of ... Director , Corporate Affairs - Brand Communications...The ideal candidate will have a strong background in scientific and corporate communications. They will be responsible for… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Medical Director , US Medical, Multiple Myeloma will report to the Senior Director ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will lead the US… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …you if you:** + Want a highly visible position with frequent interactions with Regulatory Affairs , Legal and Commercial. + Have outstanding work ethic and ... The Associate Medical Director will support the development of our medical...of our medical strategy, planning & execution of medical affairs activities. This role will provide scientific … more
- Bristol Myers Squibb (Summit, NJ)
- …group based in Summit, NJ and will be responsible for writing scientific documents including biomarker reports, regulatory documents (eg, non-clinical summaries, ... Medicine Hematology at BMS has a long-standing history of scientific rigor as evidenced by our peer-reviewed publications, delivery...+ Engage with Writers and other functions (eg, SciCom, Regulatory , Medical Affairs , Clinical, NCD) outside of… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …team advancing Regeneron's vibrant pipeline in the area of general medicine within the Regulatory Strategy group in Regulatory Affairs . The incumbent will ... prevention along with robust skills in the communication of scientific information are essential. This is an opportunity to... strategies for product development. This management position in Regulatory Affairs involves the ability to lead… more
- Sanofi Group (Morristown, NJ)
- …on millions of patients around the world. **Main Responsibilities:** The US Medical Director - New Products will provide medical and scientific guidance for the ... **Job Title:** US Medical Director - Portfolio, New Products, Innovation- Vaccines **Location** :...of Medical leaders who are a trusted source of scientific and medical information and shared insights; effective and… more
