- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and implementation of ... a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of...and other relevant sources for the prompt identification of safety signals.Lead internal and external (especially regulatory ,… more
- Merck & Co. (Rahway, NJ)
- …in the execution of clinical studies. --Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and ... changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in...an Associate Vice President in the Oncology Clinical Research Group . Under the guidance of a supervisor, the Senior… more
- Merck & Co. (Rahway, NJ)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for...execution of clinical studies. Work closely with a cross-functional group of experts in commercialization, regulatory affairs,… more
- Merck & Co. (Rahway, NJ)
- …Ensure that all activities are conducted with the highest regard for safety , quality, and regulatory compliance, aligning with the company's divisional ... Job DescriptionJob Summary: The Director , Combination Product Commercialization is a key leadership role within the Device Development and Technology Organization.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the Sr. Director , representing the Quality organization at senior levels. The Director plays a pivotal role in regulatory inspections, external audits, and ... a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of...and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of… more
- Merck & Co. (Rahway, NJ)
- …Scientists in the execution of clinical studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and ... through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe,… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Director , Clinical Pharmacology actively contributes to multi-disciplinary teams by providing innovative and ... study data and effectively communicating findings to a broad audience. The Director , Clinical Pharmacology will be relied upon to act independently, within a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …optimize, and innovate signal detection and management processes across the global safety organization. The incumbent will ensure regulatory compliance, promote ... (eg SOPs) as appropriate.Collaborate with cross-functional teams (eg, Medical Safety , Regulatory Affairs, Epidemiology) to ensure benefit-risk integration… more
- Insmed Incorporated (NJ)
- …plus.Experience with a growing medical team.Experience partnering with the HEOR group .Proven understanding of legal, regulatory , and compliance policies.Demands ... for the future of science, we're in. Are you?About the Role:The Medical Director , Medical Affairs - Dermatology role will be responsible for supporting the product… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... Scientists in the execution of clinical studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and… more
