- Novo Nordisk Inc. (Plainsboro, NJ)
- …the most diverse and collaborative groups within the organization. From health -care- provider interactions and developing and implementing regulatory strategies ... of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring external-facing… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe US Director of Precision Medicine will lead the national lab strategy, diagnostic collaboration, and partnerships across the US market. This role ... field teams associated with precision medicine, including communications and contract coordination by partnering with appropriate extended teamsIn addition, lead… more
- Genmab (Plainsboro, NJ)
- …best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical development of ... responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication LevelAct… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director , Clinical Development Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... and contributes to the site feasibility assessment from a physician's perspectiveMay provide clinical input into the eCRF (Case Report Form) design, participate in… more
- Genmab (Plainsboro, NJ)
- …to the VP, Head of Global Drug Safety & PV, the Senior Director , Global Drug Safety & Pharmacovigilance Physician serves as the safety expert accountable ... to meet corporate and patient needs is essential.ResponsibilitiesEnsure individual health care safety and welfare of individual patientsInform global safety… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... and contributes to the site feasibility assessment from a physician's perspective- May provide clinical input into the eCRF (Case Report Form) design, participate in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... and contributes to the site feasibility assessment from a physician's perspectiveMay provide clinical input into the eCRF (Case Report Form) design, participate in… more
- Daiichi Sankyo, Inc. (Seattle, WA)
- …investigations, financial assistance options, and Specialty Pharmacy issues. They will also provide education on relevant health care changes, coverage impact of ... areas centered around rare diseases and immune disorders. Summary: The Associate Director , Field Reimbursement (ADFR) is a critical front-line member of the DSI… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …quality content and review of documents supporting GLP/non-GLP/ Research submissions to Health authorities globally. Provide QA oversight of GLP/GCLP activities ... of Daiichi Sankyo, contract research organization/ vendors ensuring that outsourced obligations are...mitigation strategies are in place.Responsible to engage directly with Health authorities such as FDA, EMA, Swiss medic, and… more
- Merck & Co. (Fort Wayne, IN)
- …information and contract adherence in an effort to help the provider or system increase their immunization rates among appropriate patients and help protect ... a variety of customers within their assigned geography.-These customers may include health care providers such as physicians, nurses, pharmacists as well as quality… more
