Clinical Research Program Manager — Multisite Trials

Dormont Manufacturing Co; South Carolina; On-site; USD 66,000 - 120,000; Full time

Job summary

Medical University of South Carolina (MUSC) is seeking a Clinical Research Program Manager to oversee operations across a growing portfolio of large-scale clinical trials and multisite studies. The role includes coordinating trial startup, maintenance, and closeout, and supervising a team across multiple sites.

The position emphasizes regulatory compliance, budget management, and data integrity within FDA/GCP guidelines. Regular M-F hours with occasional evenings and weekends may be required.

Qualifications

• Five years relevant program experience.
• Experience coordinating multi-site trials.
• An MPH or other graduate degree.

Responsibilities

• Provide operational oversight across multiple trials and sites.
• Lead hiring, onboarding, and staff development activities.
• Coordinate regulatory submissions and ensure GCP compliance.
• Monitor budgets, invoices, and subcontracts for studies.
• Support data quality, study progress reporting, and logistics.

Skills

Project management

Clinical research coordination

Staff collaboration

Education

MPH or graduate degree

Bachelor's degree

Job description

Medical University of South Carolina (MUSC) is seeking a Clinical Research Program Manager to oversee operations across a growing portfolio of large-scale clinical trials and multisite studies. The role includes coordinating trial startup, maintenance, and closeout, and supervising a team across multiple sites.

The position emphasizes regulatory compliance, budget management, and data integrity within FDA/GCP guidelines. Regular M-F hours with occasional evenings and weekends may be required.