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. The first 90 days is onsite and then hybrid 4 days a week onsite.

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