**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

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.

Full time, Work at office, Flexible hours,