- University of Southern California (San Diego, CA)
- … clinical trial sites in their participant recruitment and retention efforts for multi- site clinical trials. The incumbent will be responsible for a wide ... experience/education as substitute for minimum education Minimum Experience: 2 years in on- site clinical trial monitoring. Minimum Skills: Industry experience in… more
- Merck (Rahway, NJ)
- …data-driven decision-making. Under the broad guidance of the DSCS Digital Program Mgmt Lead , the Associate Director, DSCS Digital Project Manager, will be ... **Job Description** **Position Description:** ** Associate Director, DSCS Digital Implementation Project Manager** Within the Development Sciences and Clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …and reports to the Director of PBM/Payer, Contract Strategy and Analytics. The Associate Director of Contract Strategy and Analytics is a highly skilled and ... D customer needs and to meet BMS financial targets. You will lead the evaluation and analysis of customer contracting opportunities including performing financial… more
- Henry Ford Health System (Detroit, MI)
- …urinary tract infections, central line associated bloodstream infections, and surgical site infections). The associate medical director of IPC/ASP will ... Infection Prevention and Control (IPC) and Antimicrobial Stewardship (AMS), the Associate Medical Director of IPC/AMS is responsible for implementation and oversight… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …Assurance** is responsible for providing leadership and support within Catalent's Philadelphia site . The Associate Director, QA is accountable for the group ... ** Associate Director, Quality Assurance** **Position Summary:** Catalent, Inc....providing Quality Assurance support to clinical & commercial manufacturing operations within the facility. This… more
- Merck (North Wales, PA)
- **Job Description** The Associate Director, Regulatory Affairs, supports products in the Oncology therapeutic area as part of a regulatory team. The individual will ... communication and collaboration skills and will work closely with a global regulatory lead (s) to help develop and implement a global strategy for registration and/or… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials. + Lead contributions to the preparation of material ... This position is for a qualified statistician/biostatistician to support Clinical Biostatistics with Global Development. **In this role, a typical day might… more
- Parexel (Baton Rouge, LA)
- …manage vendor + Uses Clinical Insights to manage vendors and to achieve site readiness timelines + Plans and tracks supply delivery to sites and return of ... **Job Summary:** Core member of the Clinical Trial Team (CTT), independently managing all vendor-related...risk and issues for selected categories to Trial Vendor Associate Directors Community Lead and/or and Vendor… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** GRA Device Associate **Location:** Cambridge, MA/ Morristown, NJ/ Washington DC **About the Job** Are you ready to shape the future of medicine? The ... and Manufacturing & Supply, Regulatory Health Authorities, and others. As GRA Device Associate in the GRA Device Digital and Diagnostic team you'll contribute to… more
- Bristol Myers Squibb (Madison, NJ)
- …and success of the BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, Clinical Data Management This ... their personal lives. Read more: careers.bms.com/working-with-us . **Functional Area Description** Clinical Data Management key focus is to ensure data quality,… more