On-site Clinical Trials Program Coordinator

Medical University of South Carolina; Charleston (SC); Hybrid; USD 42,000 - 54,000; Full time

Job summary

Medical University of South Carolina in Charleston, SC seeks a Program Coordinator I to support the Program Manager, Principal Investigators, and research staff in coordinating human subject activities under supervision. You will participate in day-to-day clinical research operations and serve as a liaison across stakeholders, applying regulatory knowledge to action plans.

Responsibilities include site management, study implementation, participant recruitment, scheduling visits, data collection,

Qualifications

• Bachelor's degree and one year work experience; or high school diploma (or equivalent) and 2 to 4 years work experience.

Responsibilities

• Site management and coordinating study implementation of clinical trials.
• Recruitment of study participants and scheduling study visits.
• Data collection, lab collection and processing, and maintaining regulatory files.
• Liaison for the study across stakeholders; apply research best practices and regulations.

Education

Bachelor's degree and one year work experience; or high school diploma and 2-4 years work experience

Job description

Medical University of South Carolina in Charleston, SC seeks a Program Coordinator I to support the Program Manager, Principal Investigators, and research staff in coordinating human subject activities under supervision. You will participate in day-to-day clinical research operations and serve as a liaison across stakeholders, applying regulatory knowledge to action plans.

Responsibilities include site management, study implementation, participant recruitment, scheduling visits, data collection,