Regulatory Clinical Research Coordinator - Temp

Inside Higher Ed; Chapel Hill (NC); On-site; USD 34,440 - 37,195; Full time

Job summary

A higher education institution in North Carolina is seeking a Regulatory Clinical Research Coordinator - Temp to support its Orthopaedic research program. The role involves maintaining regulatory compliance, preparing submission documents, and assisting with investigator documentation. Candidates must have a Bachelor's degree from an accredited institution and be comfortable engaging with patients. This full-time temporary position offers an hourly salary range of $25 - $27 and is estimated to last for 6 to 11 months.

Responsibilities

• Prepare, submit, and maintain regulatory documents for IRB submissions.
• Maintain complete and audit-ready regulatory binders.
• Assist with investigator documentation.
• Support study start‑up activities including regulatory approvals.

Skills

Comfortable engaging patients via phone conversations

Education

Bachelor’s degree or equivalent training and experience

Job description

Regulatory Clinical Research Coordinator - Temp

Position Title: Regulatory Clinical Research Coordinator - Temp

Department: Orthopaedics

Posting Date: 01/05/2026

Application Deadline: 01/11/2026

Position Type: Temporary Staff (SHRA), Full-Time

Hours per Week: 40

Location: North Carolina, US

Hourly Salary: $25.00 - $27.00 per hour

Estimated Duration: 6 months, not to exceed 11 months

Position Summary

The Regulatory Clinical Research Coordinator supports the growing Orthopaedic research program by assisting clinical research coordinators and principal investigators with start‑up and regulatory activities. This role maintains regulatory compliance across multiple protocols and ensures studies are conducted efficiently, accurately, and in accordance with institutional policies, federal regulations, and Good Clinical Practice.

Key Responsibilities

• Prepare, submit, and maintain regulatory documents for IRB submissions (initial submissions, amendments, continuing reviews, reportable events).
• Maintain complete and audit‑ready regulatory binders (electronic and/or paper).
• Assist with investigator documentation (CVs, licenses, CITI/GCP training records, delegation of authority logs).
• Support study start‑up activities including regulatory approvals, site readiness, and feasibility.

Minimum Education and Experience

Bachelor’s degree or equivalent training and experience. All degrees must come from accredited institutions.

Required Qualifications, Competencies, and Experience

• Comfortable engaging patients via phone conversations.

Preferred Qualifications, Competencies, and Experience

• Recruitment experience.

Campus Security Authority Responsibilities

Not Applicable.