Clinical Research Coordinator 259183

Medix™; Chevy Chase (MD); On-site; USD 65,000 - 85,000; Full time

Job summary

Medix™ is seeking a Clinical Research Professional to join our growing study team in Maryland. This on-site, full-time role supports the complete trial process with minimal supervision and requires hands-on phlebotomy, data entry, and meticulous regulatory documentation.

You will collaborate with clinic staff, principal investigators, monitors, and patients, manage patient visits, perform phlebotomy and specimen processing, and ensure IP accountability and audit readiness across EDC platforms.

Qualifications

• Certified for phlebotomy / blood draws.
• Hands-on experience operating a centrifuge for specimen processing.
• Proficiency in data entry across various Electronic Data Capture (EDC) platforms.
• Standard clinical research regulatory maintenance and audit readiness.
• Understanding of IP accountability and monitoring processes.
• Proven ability to work independently ("plug-and-play") without direct daily onsite supervision.
• Strong interpersonal skills to interface smoothly with clinic staff, principal investigators, study monitors, and patients.

Responsibilities

• Manage 1–3 patient visits per day, with periodic admin-focused days as new studies launch.
• Perform certified phlebotomy/blood draws and operate centrifuges.
• Partner with onsite clinic techs and embedded clinic staff to ensure smooth study flow.
• Input clinical trial data across various study-specific EDC platforms in a timely manner.
• Maintain standard regulatory binders and study documentation.
• Oversee IP processes (without direct drug dispensing) and host/meet with external study monitors.

Skills

Phlebotomy

Centrifuge operation

EDC data entry

Regulatory maintenance

IP accountability

Independent worker

Interpersonal skills

Job description

We are looking to add a Clinical Research Professional to a growing study team. The ideal candidate will feel comfortable in a research environment with minimal oversight and exemplify strong understanding of the full trial process. This is full time onsite M-F, competitive salary and benefits. Sponsorship is not available for this role at this time.

Duties

• Manage 1–3 patient visits per day, with periodic admin-focused days as new studies launch.
• Perform certified phlebotomy/blood draws and operate centrifuges.
• Partner with onsite clinic techs and embedded clinic staff to ensure smooth study flow.
• Input clinical trial data across various study-specific EDC platforms in a timely manner.
• Maintain standard regulatory binders and study documentation.
• Oversee IP processes (without direct drug dispensing) and host/meet with external study monitors.

Required Skills & Qualifications

• Certified for phlebotomy / blood draws.
• Hands-on experience operating a centrifuge for specimen processing.
• Proficiency in data entry across various Electronic Data Capture (EDC) platforms.
• Standard clinical research regulatory maintenance and audit readiness.
• Understanding of IP accountability and monitoring processes.
• Proven ability to work independently ("plug-and-play") without direct daily onsite supervision.
• Strong interpersonal skills to interface smoothly with clinic staff, principal investigators, study monitors, and patients.