Clinical Research Coordinator
$60,000–$80,000 year
Remote · La Vergne, Tennessee, United States or United States
La Vergne, Tennessee, United States or United StatesRemoteFull Time$60,000–$80,000 yearMid LevelBachelors DegreeUnknown
Type
Full Time
Level
Mid Level
Education
Bachelors Degree
Company size
Unknown
Job Summary
The Clinical Research Coordinator at Civia Health manages all aspects of Phase 2–4 clinical trials, ensuring compliance and patient safety while utilizing advanced technology to enhance trial efficiency. Requires a Bachelor's degree and at least 3 years of relevant experience.
Required Qualifications
- Minimum 3 years of experience coordinating Phase 2–4 clinical trials in a site, SMO, or academic research setting
- Strong interpersonal skills for effective collaboration with patients, investigators, and sponsors
- Excellent organizational skills
- Attention to detail
- Ability to prioritize multiple studies
- Knowledge of GCP, FDA regulations, and clinical trial conduct
Desired Qualifications
- Certified Clinical Research Coordinator (CCRC) preferred
- Experience with eSource, eConsent, and electronic Investigator Site Files (eISF) systems
- Proficient in Microsoft Office Suite and clinical trial management systems (CTMS)
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.