Job Description

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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