Senior Research Coordinator

About the role

This is a fully on-site position in Lexington, Kentucky. Are you ready to accelerate your career in clinical research? 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.

Responsibilities

• Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
• Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
• Experience working with participants as a CRC I (minimum of 1-3 years) or CRC II (minimum of 3 years).
• Gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities.
• Be part of a supportive team that values initiative, adaptability, and continuous learning.

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.
• Strong written and verbal communication skills, with attention to detail and time management.
• Comfortable using CTMS, eCRFs, and Microsoft Office tools.

Benefits

Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish.

Pay

The potential base pay range for this role, when annualized, is $44,300.00 - $110,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

Schedule

Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.