Opportunity Description
Job Description
A client of Insight Global’s is seeking a Clinical Research Coordinator (CRC B/C) to support the day‑to‑day operations of multiple investigator‑initiated and industry‑sponsored dermatology clinical trials. On a daily basis, this individual will screen clinic schedules and medical records to identify eligible patients, conduct informed consent discussions, and coordinate protocol‑required study visits and assessments. They will manage visit documentation, source documents, and regulatory binders; enter and review data in systems such as REDCap or sponsor EDC platforms; and ensure compliance with GCP, IRB, and institutional requirements. The coordinator will handle specimen collection and processing, monitor participants for adverse events, and support safety reporting as needed. This role requires independent management of 4–5 active studies, regular communication with investigators, sponsors, and CROs, and close collaboration with a growing, team‑based clinical resea...
A client of Insight Global’s is seeking a Clinical Research Coordinator (CRC B/C) to support the day‑to‑day operations of multiple investigator‑initiated and industry‑sponsored dermatology clinical trials. On a daily basis, this individual will screen clinic schedules and medical records to identify eligible patients, conduct informed consent discussions, and coordinate protocol‑required study visits and assessments. They will manage visit documentation, source documents, and regulatory binders; enter and review data in systems such as REDCap or sponsor EDC platforms; and ensure compliance with GCP, IRB, and institutional requirements. The coordinator will handle specimen collection and processing, monitor participants for adverse events, and support safety reporting as needed. This role requires independent management of 4–5 active studies, regular communication with investigators, sponsors, and CROs, and close collaboration with a growing, team‑based clinical resea...
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