Clinical Research Nurse Coordinator, On-Site, Jefferson City, Missouri
About The Position
This is a fully on-site position in Jefferson City, Missouri Are you ready to take your nursing expertise beyond traditional patient care? At Avacare Clinical Research Network , we’re driving innovation through clinical trials that change lives. As a Clinical Research Nurse Coordinator , you’ll play a vital role in advancing medical breakthroughs while developing specialized skills in the growing field of clinical research. Why Join Avacare? Impactful Work: Every study you coordinate brings us closer to life-changing treatments. Expand Your Horizons: Move beyond bedside care and gain expertise in protocol management, regulatory compliance, and patient advocacy in research settings. Collaborative Culture: Work with a passionate team committed to excellence and innovation. Dynamic Environment: Be part of cutting-edge studies in a fast-paced, rewarding setting. Job Overview: Partner with investigators to prepare and execute clinical studies. Recruit, screen, and guide patients through trial participation. Perform and oversee clinical procedures (IV placement, phlebotomy, ECG, spirometry, etc.). Ensure compliance with GCP/ICH standards and regulatory requirements. Monitor patient safety and report adverse events promptly. Maintain accurate documentation and support audits/inspections. Train and mentor new team members while advocating for patient well-being.
Requirements
- RN, LPN, or LVN (active and in good standing).
- 3+ years in clinical research or equivalent training.
- Strong knowledge of clinical trials, GCP, and medical terminology
- Proficiency in clinical procedures including placing IV's, Phlebotomy, EKG's, obtaining patient vitals etc.
Nice To Haves
- CCRC or CCRP certification
Responsibilities
- Partner with investigators to prepare and execute clinical studies.
- Recruit, screen, and guide patients through trial participation.
- Perform and oversee clinical procedures (IV placement, phlebotomy, ECG, spirometry, etc.).
- Ensure compliance with GCP/ICH standards and regulatory requirements.
- Monitor patient safety and report adverse events promptly.
- Maintain accurate documentation and support audits/inspections.
- Train and mentor new team members while advocating for patient well-being.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees
