Onsite Clinical Research Coordinator — Phlebotomy (Contract)

Medix™; Potomac (MD); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Health benefits

Dental

Vision

401k

Job summary

Medix is seeking a Clinical Research Coordinator in Potomac, MD for a 40-hour workweek, Monday to Friday. This 100% onsite contract position coordinates clinical trial protocols from start-up to close-out, with data collection and regulatory activities handled in compliance with FDA and ICH-GCP guidelines.

The role requires phlebotomy experience and local residency; the contract ends January 2027 with no permanent opportunities.

Qualifications

• Phlebotomy experience required.
• Must be local to Potomac, MD area.
• Contract ends January 2027; no permanent role.
• On-site role; 40 hours/week, M-F.

Responsibilities

• Coordinate clinical research protocols from start-up to close-out.
• Manage data collection, entry, and queries in EDC systems.
• Liaise with sponsor/CRO; may handle regulatory submissions.
• Participate in site feasibility, qualification visits and initiation visits.
• Assist in recruiting clinical trials to site.

Skills

Phlebotomy

Tools

EDC systems

Job description

Medix is seeking a Clinical Research Coordinator in Potomac, MD for a 40-hour workweek, Monday to Friday. This 100% onsite contract position coordinates clinical trial protocols from start-up to close-out, with data collection and regulatory activities handled in compliance with FDA and ICH-GCP guidelines.

The role requires phlebotomy experience and local residency; the contract ends January 2027 with no permanent opportunities.