- Merck & Co. (North Wales, PA)
- …technology and applying rigorous scientific and ethical standards.The Senior Director ( Senior Principal Scientist ) has primary responsibility for the ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety...to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical… 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 ... **Job Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety...to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical… more
- Boehringer Ingelheim (Ridgefield, CT)
- …as needed. In addition, integrated safety assessments may also be presented to senior management at milestone review meetings. The incumbent may also serve as, or ... pro-actively manage safety liabilities. + Deliver updates to Project Teams and Senior Level management with context of overall project goals and impact on… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. The purpose of the Associate/ Senior Associate/ Principal Associate - MQO is to support the development and ... + Understand the roles and responsibilities of the EU Qualified Person for Pharmacovigilance (EU QPPV), if applicable. + Serve as an IT systems business quality… more
