- Merck & Co. (North Wales, PA)
- …and applying rigorous scientific and ethical standards.The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new… more
- Arvinas (New Haven, CT)
- …more information, please visit www.arvinas.com . **Position Summary** The Clinical Scientist is responsible for providing scientific support for all Global Clinical ... both internal and external to the company. The Clinical Scientist needs to possess the ability to think creatively,...CT, or remote from a location within the US ** Principal Responsibilities** Key responsibilities of this role include, but… more
- Merck (Rahway, NJ)
- …and applying rigorous scientific and ethical standards. The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and ... **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new… more
- Boehringer Ingelheim (Ridgefield, CT)
- …& Clinical Pharmacology, CMC, Regulatory Affairs, Patient Safety and Pharmacovigilance to implement discovery and development toxicology strategies that enable ... the progression of optimized drug candidates. + When appropriate, take lead to develop plan and lead sub-team for investigative studies to support investigations on mechanisms of toxicity. + Serve as NDS Therapeutic Area lead, and/or provide guidance and… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. The purpose of the Associate/Senior Associate/ Principal Associate - MQO is to support the development and implementation of ... + Understand the roles and responsibilities of the EU Qualified Person for Pharmacovigilance (EU QPPV), if applicable. + Serve as an IT systems business quality… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …plan, working closely with Disease Area Head, Clinical Development Lead, Clinical Scientist . and other functional areas such as GCO, biostats, regulatory, ... pharmacovigilance . The Director will be a key contributor to...in the academic environment and/or acted as an assistant Principal Investigator or Principal Investigator. + May… more
