What are the responsibilities and job description for the Clinical Research Coordinator - 182825 position at Medix™?
Clinical Research Coordinator (Onsite – Morgantown, WV)
We are seeking an experienced Clinical Research Coordinator to lead study startup and trial execution. This role is ideal for a self-starter who can independently manage regulatory processes and help build research operations from the ground up.
Key Responsibilities
- Oversee full study lifecycle: startup, regulatory, execution, and closeout
- Prepare IRB documents, 1572s, DoA logs, budgets, and contracts
- Create and manage paper source documents using site templates
- Perform phlebotomy and basic patient-facing tasks
- Attend routine clinic visits to extract relevant data and update study documentation
- Act as the primary research lead onsite, working closely with clinic leadership
Qualifications
- 2 years of industry-sponsored clinical research experience
- Strong regulatory/startup knowledge
- Experience supporting Phase 2–3 studies
- Phlebotomy experience preferred
- Bachelor’s degree preferred (Associate’s with experience considered)
Schedule & Details
- Fully onsite in Morgantown, WV
- Flexible schedule: 4x10s (Mon–Thurs) or 5x8s
- Contract-to-Hire (1,040 Hours)
- Pay: dependent on experience
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