A large healthcare company is looking to hire a Clinical Research Coordinator in Abington, PA. This person must have a car as they are going back and forth between the cancer center and hospital (few miles). This person will run portions of clinical trials, process research samples, obtain signatures for informed consent, central lab management, data management, complete expectancy reports, and monitor visit preparation, all in accordance with GCP.

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Required Skills & Experience

I have a background in Clinical Research and working directly with patients, ordering scans and labs, working with monitors, and organizing and maintaining all patient data.
- Experience working with protocols
- Experience managing all aspects of clinical research regulation for patients from protocol inception to completion and tracking quality metrics

Nice to Have Skills & Experience

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.