Senior Research Program Coordinator for Clinical Trials

MUSC Health; Charleston (SC); On-site; USD 60,000 - 80,000; Full time

Job summary

MUSC Health in Charleston, SC is seeking a Research Program Coordinator II–Journeyman to lead and oversee complex research studies. This role includes conducting research activities, managing industry-sponsored trials, and ensuring compliance with regulatory requirements.

The ideal candidate will have a Bachelor's degree and three years of experience. Responsibilities also include liaisons with stakeholders and maintaining regulatory documentation throughout the project lifecycle.

Qualifications

• Three years of relevant program experience in research studies.
• Ability to manage complex research projects and comply with regulations.
• Strong communication skills for liaising with various stakeholders.

Responsibilities

• Lead day-to-day operations of multiple research studies.
• Coordinate data management and reporting to stakeholders.
• Ensure compliance with IRB and FDA requirements.
• Recruit and enroll research subjects as per protocol timelines.

Skills

Research coordination

Data management

Regulatory compliance

Communication

Team collaboration

Education

Bachelor's degree

Job description

MUSC Health in Charleston, SC is seeking a Research Program Coordinator II–Journeyman to lead and oversee complex research studies. This role includes conducting research activities, managing industry-sponsored trials, and ensuring compliance with regulatory requirements.

The ideal candidate will have a Bachelor's degree and three years of experience. Responsibilities also include liaisons with stakeholders and maintaining regulatory documentation throughout the project lifecycle.