Senior Research Coordinator
About The Position
This is a fully on-site position in Lexington, Kentucky. Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. At Avacare, CRCs wear more hats than in traditional research settings. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. Avacare offers a unique environment where your contributions matter and your career can flourish.
Requirements
- Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
- Solid understanding of site operations and the drug development process.
- Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
- Strong written and verbal communication skills, with attention to detail and time management.
- Comfortable using CTMS, eCRFs, and Microsoft Office tools.
Responsibilities
- Manage 2–6 trials of varying complexity
- Perform clinical procedures
- Lead study coordination from start to finish
- Work closely with investigators, sponsors, and monitors
- Mentor junior staff
- Contribute to internal training
- Obtain vital signs
- Perform phlebotomy
- Conduct ECGs
- Process lab specimens
- Patient recruitment
- Informed consent
- Regulatory documentation
- Site audits
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed
