Description
Join Avacare, a dynamic Site Management Organization (SMO), as a Clinical Research Coordinator (CRC) in Lexington, Kentucky. You'll gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment.
At Avacare, CRCs manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish. You'll work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
Responsibilities and Benefits:
- Manage multiple trials and perform clinical procedures
- Lead study coordination, patient recruitment, and informed consent
- Work closely with investigators, sponsors, and monitors
- Mentor junior staff and contribute to internal training
- Part of a supportive team that values initiative, adaptability, and continuous learning
- Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO
Qualifications:
- 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
- Experience as a CRC: 1-3 years (CRC I) or 3+ years (CRC II)
- Strong written and verbal communication skills, with attention to detail and time management
- Comfortable using CTMS, eCRFs, and Microsoft Office tools
The potential base pay range for this role is $44,300.00 - $110,500.00 per year.