Job Title : Clinical Research Coordinator
Job Description
Recruit, screen, and enroll subjects into clinical trials. Explain the informed consent process to participants. Document adverse events accurately.
Collect and manage study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.
Prepare applications for the Institutional Review Board (IRB).
Hard Skills
- clinical research
- research coordinator
- consenting patients
Job Type
This is a Contract-to-Hire position with a duration of 6 Month(s).
Work Site
This is a hybrid position requiring some days on-site in Philadelphia, Pennsylvania and some days remote.
Work Environment
Combination of an office and hospital / outpatient surgery setting. Very fast-paced and high-volume workload involving industry and investigator studies.
The position involves working within one of the most prestigious academic research institutes in the world, utilizing state-of-the-art equipment, and participating in high-profile studies with large, well-known sponsors.
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Promote good clinical practice in the conduct of clinical investigations, including possessing and in depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection. Coordinate and conduct clinical studies, including subject recruit...
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