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

SGliaURlb2l4YVdyOFJLczcwUysvT1JtZ0E9PQ==
  • 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,

Similar Jobs

Dropoff, Inc.

Driver Contractor Job at Dropoff, Inc.

 ...proprietary technology platform and trusted, professional delivery drivers, Dropoff seamlessly becomes an extension of any business and a...  ...looking fordriversin the West Henrietta/Rochester area for medical deliveriesboth local and long haul. You'll be transporting... 

Grey Staffing

Senior Electrical Power Engineer Job at Grey Staffing

 ...Overview The Sr. Member of Technical Staff is responsible for electrical design of next generation high reliability undersea products...  ...a team of electrical, mechanical, optical and reliability engineers to design high reliability fault tolerant circuit to operate in... 

The 3M Company

Full Time Warehouse Operator 2nd Shift Job at The 3M Company

3 M is seeking a Full-Time Warehouse Operator located in DeKalb, IL. This position is Full-time on 2nd Shift. Hours are Monday-Friday 2:30 pm-10:30 pm Job Description: The person hired for the position of Warehouse Operator will work in our 3 M Distr Warehouse Operator,... 

Trinity Health Mid-Atlantic - Trinity Health Mid-Atlantic Me...

Cardiology - Physician Job at Trinity Health Mid-Atlantic - Trinity Health Mid-Atlantic Me...

 ...Fitzgerald Hospital's cardiology team, providing inpatient consults and office-based clinical care including various imaging techniques and...  ...~ Inpatient consults & office-based clinical care, echo, TEE, nuclear cardiology, vascular imaging, CPET ~ EMR system integration... 

Outlier AI

Research Assistant (Remote) Job at Outlier AI

 ...data has led to AI advancements for the world's leading AI labs and large language model builders. Weve built a best-in-class remote work platform for our freelance contributors to provide valuable, specialized skills, and we in turn strive to provide them with a...