- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primary source of medical accountability and oversight for one or more clinical trials. Matrix management responsibilities across the internal and external network. ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Summary: This position is responsible for enabling the on-time delivery of clinical supplies across the DSI portfolio. This role is primarily responsible for ... more
- Merck & Co. (South San Francisco, CA)
- …Education: Master's in biology, pharmacology, medicine or related fields with four (4) years of relevant experience listed below Ph.D. or MD in biology, pharmacology, ... more
- Merck & Co. (Rahway, NJ)
- …Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of ... more
- Merck & Co. (Rahway, NJ)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our ... more
- Merck & Co. (North Wales, PA)
- …of TMS is to provide statistical support for the pharmacology components of all clinical trials in our company's clinical development pipeline. Also in scope ... more
- Aequor (Atlanta, GA)
- Job Title: Clinical Evaluations Specialist - Regulatory Documentation - Vision Science/ Ophthalmology background is preferred. REMOTE ROLE - candidates must be ... more
- Novo Nordisk Inc. (Austin, TX)
- …The EDCS must achieve sales goals by utilizing a patient-centric and clinical approach to engaging their customers and promoting Novo Nordisk's portfolio of ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …The Manager, Data Management is accountable for end-to-end delivery of clinical data management services for assigned studies, collaborating with study teams, ... more
- Merck & Co. (North Wales, PA)
- …investigators essential to insight collection and participation in Our Company's clinical development programIdentify new and emerging science in areas important to ... more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... more
- Merck & Co. (North Wales, PA)
- …:This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Affairs activities including strategy, communications, and medical affairs directed clinical activities across the oncology portfolio. The position has leadership ... more
- Merck & Co. (Boston, MA)
- …Translational Medicine at our Research Division is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery ... more
- Novo Nordisk Inc. (San Diego, CA)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... more
- Novo Nordisk Inc. (Akron, OH)
- …centers, HCPs and other stakeholders in a given geography. Utilizing approved clinical resources to support provider efforts to deliver appropriate care for ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …patient selection and patient enrichment strategies for programs across the clinical portfolio. The successful candidate for this position will provide technical ... more
- Merck & Co. (Boston, MA)
- …DescriptionBrief Description of PositionTranslational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration ... more
- Merck & Co. (Boston, MA)
- …of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician-scientist with a proven ... more
- Beckman Coulter Diagnostics (Miami, FL)
- …tools that address the world's biggest health challenges. The Senior Clinical Research Associate for Beckman Coulter Diagnostics is responsible for monitoring ... more
