- Boehringer Ingelheim (Ridgefield, CT)
- …programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , DRA Product Labeling will lead and manage the coordination of ... to support labeling initiatives in compliance with Corporate and local regulatory requirements. The AD, DRA Product Labeling Operations will provide training,… more
- RWJBarnabas Health (New Brunswick, NJ)
- Director , Cardiac Diagnostics (RN) - New Brunswick, NJReq #:0000151612 Category:Leadership Status:Full-Time Shift:Day Facility:RWJ New Brunswick Department:Cardiac ... One Robert Wood Johnson Place, New Brunswick, NJ 08901 Job Title: Director Location: RWJ New Brunswick Department: Cardiac Catheter Lab Req#: 0000151612 Status:… more
- Merck (De Soto, KS)
- …Description** Join our Global Engineering Solutions leadership team as the Associate Director , Project Technical Lead! The Associate Director will drive the ... project management expertise, exemplary communication and collaboration skills with proven regulatory and quality compliance experience. Reporting to the GES Animal… more
- University of Rochester (Dansville, NY)
- …year **Description** **Overview** The Department of Family Medicine seeks an Associate Director of Rural Residency to join our team, providing oversight and clinical ... professional development and a tradition of mentorship. **Role Summary** The Associate Director will work closely with the Residency Program Director to… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director , Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures scientific ... projects through early and/or late phase development. Reports to the Director , Clinical Sciences Hematology, Clinical Sciences and collaborates closely with Medical… more
- Sanofi Group (Cambridge, MA)
- …project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, ... **Job title** : Clinical Research Director , I and I, Pulmonology **Location:** Cambridge, MA...sections of integrated development plans, and submission dossiers for regulatory approval + Support drug registrations (contribution… more
- Bristol Myers Squibb (Princeton, NJ)
- …data analysis, interpretation, and reporting + Collaborates on cross-functional drug development teams, regulatory submissions, and departmental initiatives; ... and model informed drug development (MIDD) approaches + Track record of regulatory interactions and deliverables, eg, IND, NDA, BLA and MAA filings. + In-depth… more
- Otsuka America Pharmaceutical Inc. (Atlanta, GA)
- …to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD is responsible for all ... of drugs and unmet medical needs. + Formulating a rationale to develop the drug in accordance with a clinical and regulatory strategy. + Working with… more
- HCA Healthcare (Richardson, TX)
- …about Galen! (https://galencollege.edu/about) **Position Overview:** The Associate Program Director provides oversight and direction to applicants, enrolled ... students, faculty, and staff. The Associate Program Director will be responsible for the student-focused operational success of the program(s) in conjunction with… more
- CVS Health (Springfield, IL)
- …CVS Health, a Fortune 6 company, has an outstanding opportunity for a Medical Director (Medical Affairs). This is a remote based, work from home opportunity. The ... Quality activities, consultative support to the P&T process, formulary development, drug information services and pipeline activities, and provision of clinical… more