A large healthcare company is looking to hire a Clinical Research Coordinator in Philadelphia, PA. This person will be running portions of clinical trials, assisting with orientation and training, obtaining signatures for informed consent, central lab management, data management, completing expectancy reports, monitors visit preparation, submitting low institutional risk trials, and tracking IRB submission and approvals; all in accordance with GCP.
-Background working in Clinical Research and working directly with patients, ordering scans, labs, and working with monitors. Organizing and maintaining all patient data.
-Experience creating source documents
-Experience working with protocols
- Prepare and submits materials for the IRB
-Experience managing all aspects of clinical research regulation from protocol inception to completion; and tracking quality metrics
Oncology Clinical Trial Experience
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.