Participant Recruitment Specialist - Clinical Research

Medical University of South Carolina; Orleans Estates (SC); On-site; USD 45,000 - 77,000; Full time

Job summary

Medical University of South Carolina seeks a Recruitment Coordinator to manage day-to-day recruitment of research subjects across multiple disease areas. The role collaborates with Clinical Research Program leadership, investigators, coordinators and assistants to advance medical knowledge and patient care.

40 hours/week, onsite. The successful candidate will implement subject recruitment activities, screen participants, and coordinate study visits while maintaining accurate records and

Qualifications

• Bachelor's degree required and at least 1 year of relevant program experience.
• Experience supporting recruitment for clinical studies and enrollment goals.
• Strong communication and organization skills with attention to detail.

Responsibilities

• Identify and recruit potential participants using EHR reports, screening clinics, and referrals.
• Conduct pre-screening and eligibility assessments per study protocols and obtain consent when applicable.
• Contact patients to introduce studies, assess interest, and provide education on procedures.
• Coordinate and schedule screening visits with investigators and study teams.
• Track recruitment activity and maintain accurate records in shared databases.
• Collaborate with providers and research staff to support enrollment and follow-up workflows.

Skills

Recruitment coordination

EHR screening

Participant outreach

Education

Bachelor's degree

Tools

Microsoft Planner

Job description

Medical University of South Carolina seeks a Recruitment Coordinator to manage day-to-day recruitment of research subjects across multiple disease areas. The role collaborates with Clinical Research Program leadership, investigators, coordinators and assistants to advance medical knowledge and patient care.

40 hours/week, onsite. The successful candidate will implement subject recruitment activities, screen participants, and coordinate study visits while maintaining accurate records and