- Virtua Health (Marlton, NJ)
- …*This is not a remote position* Summary:Coordinates and participates in clinical research studies conducted by principal investigators. Acts as a liaison ... Position Qualifications Required: Required Experience: 2-5 years data management clinical research experience, and strong administrative experience. Strong… more
- Penn Medicine (Plainsboro, NJ)
- …_for more information regarding our amazing benefits package._ Summary: + The Oncology Research Coordinator is responsible for the day-to-day research ... regulatory authorities, sponsors, cooperative groups, and other stakeholders. + The Oncology Research Coordinator is responsible to ensure that all new patients… more
- Eurofins (West Point, PA)
- …& Operations (GTCO), Distribution Planning, Master Planning, site shipping personnel, and Clinical Research stakeholders across global locations. + Receive & ... quality requirements Order Fulfillment-specific Responsibilities: + Partner with multiple research locations, clinical sites, primary/secondary depots, and… more
- Merck (Trenton, NJ)
- …**Required Experience and Skills:** + Minimum of 6 years of relevant experience in clinical research , including at least 2 years of direct experience with ... business critical that our Company receives consistent, accurate, high-quality data from clinical trials conducted worldwide. In collaboration with the Clinical … more
- Cardinal Health (Trenton, NJ)
- **_What Individualized Care contributes to Cardinal Health_** Clinical Operations is responsible for providing clinical specialties support and expertise in the ... areas of advice and consulting, research and patient care to internal business units and...our normal business hours of Monday-Friday, 7:00am- 7:00pm CST. ** REMOTE DETAILS:** You will work remotely, full-time. It will… more
- Merck (North Wales, PA)
- …reporting and MS Office tools. **_Preferred_** + Five years of experience in clinical research / clinical development. + Excellent teamwork and leadership ... Data Management, Pharmacovigilance, Essential Document Management, and Investigator/ Study Coordinator roles/ responsibilities. + Experience with critical clinical… more