Clinical Research Coordinator - 247687 Job at Medix™, La Vergne, TN

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  • Medix™
  • La Vergne, TN

Job Description

**Seeking a FULL TIME Clinical Research Coordinator for a brand new site in La Vergne, TN. Phlebotomy skills are a MUST!**

Overview

What You’ll Do

Clinical Trial Coordination

  • Coordinate and manage all aspects of assigned Phase 2–4 clinical trials from site initiation to close-out.
  • Conduct study visits, including obtaining informed consent, performing protocol-required procedures, and collecting source data using eSource systems.
  • Ensure timely and accurate entry of study data into electronic case report forms (eCRFs).

Technology & Documentation

  • Utilize eSource, eConsent, eISF, and other clinical trial software platforms to maintain complete, accurate, and regulatory-compliant study records.
  • Support site readiness and compliance with 21 CFR Part 11, ICH GCP, and sponsor SOPs.

Regulatory Compliance

  • Maintain up-to-date regulatory documents and study binders (electronic and/or paper as required).
  • Assist with preparation for sponsor, CRO, or regulatory audits.

Patient Engagement & Safety

  • Recruit, screen, and enroll study participants according to protocol inclusion/exclusion criteria.
  • Ensure ongoing patient safety by monitoring for adverse events and reporting per protocol.

Collaboration & Support

  • Serve as the primary point of contact for sponsors, CROs, monitors, and other site staff.

Support training and mentoring of new CRC staff as assigned.

  • Provide on-site support at additional study locations when required (occasional travel).
  • Occasional travel may be required for audits, site visits, or team meetings.?

What We Offer

  • Competitive compensation
  • Medical, dental, and vision insurance
  • Generous PTO and paid holidays
  • Flexible scheduling options
  • Professional development and continuing education support
  • A mission-driven team that values respect, inclusion, and innovation

Ready to Make an Impact?

  • Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact.
  • Startup Energy, Proven Expertise: Work fast, adapt quickly, and help build something new; guided by seasoned visionary?professionals who’ve seen what needs to change.
  • People First Culture: We care deeply about our patients, participants, and each other. Collaboration, transparency, and bold, straight-talking are core to how we work.
  • Invested in Your Growth: We don’t just hire for today; we’re building the leaders and change makers of tomorrow.?

3-5 Must Have Skills/Qualifications

What You Bring

  • Strong interpersonal skills for effective collaboration with patients, investigators, and sponsors.
  • Excellent organizational skills, attention to detail, and ability to prioritize multiple studies.
  • Proficient in Microsoft Office Suite and clinical trial management systems (CTMS).
  • Experience with eSource, eConsent, and electronic ISF systems strongly preferred.
  • Minimum 3 years of experience coordinating Phase 2–4 clinical trials in a site, SMO, or academic research setting.
  • Certified Clinical Research Coordinator (CCRC) a plus.

Knowledge of GCP, FDA regulations, and clinical trial conduct.

Job Tags

Full time, Work at office, Flexible hours,

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