Clinical Research Coordinator II: Impactful Trials

Prisma Health; Greenville (SC); On-site; USD 55,000 - 75,000; Full time

Job summary

Prisma Health in Greenville, SC seeks a Clinical Research Coordinator to implement and manage day-to-day clinical trial activities, educate staff, participants, and caregivers, and ensure accurate data flow across studies.

You will monitor progress, ensure protocol compliance, coordinate data submissions, and communicate updates to investigators, regulatory offices, and study teams. This role requires strong knowledge of GCP and regulatory requirements.

Qualifications

• Bachelor's degree required; health sciences or related field preferred.
• Minimum two years of research experience in pharmaceutical, academic, device, NIH, investigator-initiated studies or registry trials.
• Experience with Good Clinical Practice (GCP) and regulatory requirements.
• Ability to interpret medical records and manage high-quality source documentation.

Responsibilities

• Coordinate day-to-day study operations and contribute to program growth.
• Monitor progress and ensure protocol compliance and regulatory adherence.
• Manage participant visits and carry out required procedures.
• Assist with protocol development, literature reviews, and data collection tools; coordinate regulatory submissions.
• Support sponsor-initiated and industry-sponsored trials by implementing sponsor protocols and timelines.
• Communicate study progress, amendments, and regulatory activities to investigators and study staff.

Skills

GCP knowledge

Regulatory compliance

Protocol execution

Medical records interpretation

Data abstraction & quality

Professional development

Education

Bachelor's Degree in Health Sciences or related field

Job description

Prisma Health in Greenville, SC seeks a Clinical Research Coordinator to implement and manage day-to-day clinical trial activities, educate staff, participants, and caregivers, and ensure accurate data flow across studies.

You will monitor progress, ensure protocol compliance, coordinate data submissions, and communicate updates to investigators, regulatory offices, and study teams. This role requires strong knowledge of GCP and regulatory requirements.