- The Coca-Cola Company (Whitestone, NY)
- …relevant science discipline required. **Job Description Summary** : The Director , Scientific and Regulatory Affairs Compliance and Innovation develops, ... improves, and drives compliance to all Regulatory requirements at BODYARMOR. In addition, this role also...5 to 7 years of experience in a similar Regulatory role, food and beverage experience preferred. + … more
- AbbVie (Florham Park, NJ)
- …strategy. + Must possess excellent oral and written English communication skills. Scientific Director Qualifications: + Advanced Degree PhD or PharmD. Additional ... scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions (HCPs, Patients and… more
- AbbVie (Florham Park, NJ)
- …including regulatory guidelines to meet customer needs. Qualifications Associate Scientific Director Qualifications + Bachelor's Degree in the sciences. ... level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and… 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
- Merck (Rahway, NJ)
- …Drug-Device Combinations CMC (Chemistry, Manufacturing & Controls), you will report to the Director of Device Regulatory Affairs for Autoinjector Development ... Support device design control activities and documentation reviews + Provide evaluations of regulatory state of affairs of any devices and combination products,… 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
- 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
- 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
- Merck (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
- Cline Davis & Mann (New York, NY)
- **Overview** The VP, Medical Director is responsible for leading the agency team in the understanding and application of scientific /clinical account data. A high ... is required. He/she, in collaboration with his/her team, will prepare scientific and strategic analyses of data, conduct research and disseminate brand/category… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director … more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to ... As a senior member of Medical Science, the Senior Director , oncology group, Medical Science - Early Stage will...for the company, drawing on expertise in clinical and regulatory strategy and requirements, both local and international, related… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …as needed + Partners cross-functionally with departments such as Regulatory Affairs , Toxicology, CMC/Formulations, Biostatistics, Legal, Marketing, ... documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Senior Director , Clinical Development will… more
- Pfizer (New York, NY)
- …The medical director works closely with other functions such as regulatory affairs , pharmacovigilance, biostatistics, and medical affairs to ensure ... that the clinical development program meets the scientific , ethical, and regulatory standards. The medical director also provides medical expertise and… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …Reporting into the Senior Director of the Medical Science Early-Stage, the Director , MSES will lead clinical and scientific aspects of Early Development ... 2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to… more
- AbbVie (Florham Park, NJ)
- …including Clinical Development Operations, Clinical Development, Biostatistics, Pharmacovigilance, and Regulatory Affairs , to ensure the integration and accuracy ... trial. Our operational model is exemplified through execution and innovation. The Director of Clinical Data Strategy & Operations (CDSO) oversees the Oncology… more
- Helsinn Therapeutics (US), Inc. (Iselin, NJ)
- …HTU activities. + Collaborate with US leadership (Legal, Sales, Marketing, Medical & Scientific Affairs , and Human Resources) on compliance matters to ensure ... Director of Compliance Compliance Iselin, New Jersey Apply...and providing compliance guidance to commercial and medical and scientific affairs departments. Prior supervisory experience is… more
- Merck (Rahway, NJ)
- …Direct and manage all communications across the portfolio and pipeline, including regulatory approvals, governing bodies, publications of scientific data and ... **Job Description** The Executive Director , Global Pharma Communications is responsible for leading,...the company's pipeline, including during late-stage development, distribution and regulatory milestones, in a manner that reflects the company's… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to ... and creating hope for all facing illness. The Associate Director , Quality Management System will be responsible for supporting...and processes are robust and complaint to meet the regulatory and end user needs. **Responsibilities** + Support and… more