CareerPlanGet AI match score →

Clinical Research Coordinator (On-site)

Wilmington, NC, us💼 Full-time🗓 2026-07-07 → 2026-07-31

Core

Coordinate daily clinical trial activities, manage participant screening, maintain case report forms, and ensure compliance with research protocols and regulations.

Role type

Senior Clinical Research Coordinator (Mentoring & Oversight)

Builds

Clinical trial data and documentation for biopharmaceutical and medical device studies

Domain

Clinical Research / Healthcare / Life Sciences

Deliverable

client delivery

Required skills

Clinical trial knowledge, GCP certification, phlebotomy, medical assistant/LPN/RN experience, data entry, regulatory compliance (CFR/HIPAA), study start-up/maintenance/close-out

Preferred skills

Advanced CRC certification, mentoring experience, complex protocol interpretation

Technologies

Case report forms, patient databases

Responsibilities

Screen and review potential study participant eligibility; maintain case report forms, charts, and documentation; mentor and oversee research assistants; collect and enter clinical data; assist with study start-up, maintenance, and close-out

Seniority

Mid-level, hands-on IC with mentoring responsibilities

Sourced via smartrecruiters · Listed on CareerPlan, which tracks 70,000+ jobs from 20+ sources.
Apply on SmartRecruiters ↗