Clinical Research Program Assistant - Transplant Studies

experiencedAlliedHealth; Charleston (SC); On-site; USD 38,000 - 61,000; Full time

Job summary

Medical University of South Carolina (MUSC) is seeking a Clinical Research Assistant to coordinate investigator-initiated transplant studies for the Department of Surgery, ensuring adherence to FDA CFR, Good Clinical Practices, and MUSC IRB regulations protecting human subjects.

The role includes conducting study visits, obtaining informed consent, screening patients, completing case report forms, data entry into study databases, and maintaining accurate documentation within a 40-hour work week.

Qualifications

• High school diploma and at least four years of relevant program experience (bachelor’s degree may substitute).
• Experience coordinating investigator-initiated studies is a plus.
• Familiarity with FDA CFR, GCP, and IRB regulations is preferred.

Responsibilities

• Coordinate transplant study activities per protocol.
• Obtain and document informed consent.
• Screen and prescreen potential participants for studies.
• Complete case report forms and other source documents on time.
• Enter data into study databases and resolve queries in the EDC system.

Skills

Clinical research coordination

Informed consent

Data entry

Education

High school diploma + 4 years relevant program experience

Bachelor’s degree may substitute required experience

Job description

Medical University of South Carolina (MUSC) is seeking a Clinical Research Assistant to coordinate investigator-initiated transplant studies for the Department of Surgery, ensuring adherence to FDA CFR, Good Clinical Practices, and MUSC IRB regulations protecting human subjects.

The role includes conducting study visits, obtaining informed consent, screening patients, completing case report forms, data entry into study databases, and maintaining accurate documentation within a 40-hour work week.