Senior Research Coordinator
$44,300–$110,500 year
On-siteLexington, Kentucky, United States or Versailles, Kentucky, United States
Job Summary
Manage 2–6 trials of varying complexity by handling patient recruitment, informed consent, regulatory documentation, and site audits. Perform clinical procedures including obtaining vital signs, phlebotomy, ECGs, and lab specimen processing while coordinating with investigators, sponsors, and monitors. Lead study coordination from start to finish and mentor junior staff within a collaborative Site Management Organization environment. This fully on-site position in Lexington, Kentucky offers exposure to diverse therapeutic areas and prepares candidates for future roles in clinical operations and monitoring.
Required Qualifications
- CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants
- CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants
- Solid understanding of site operations and the drug development process
- Strong written and verbal communication skills
- Attention to detail
- Time management
- Comfortable using CTMS, eCRFs, and Microsoft Office tools
- Hands-on experience in obtaining vital signs
- Performing phlebotomy
- Conducting ECGs
- Processing lab specimens
- Must be able to lift 50 lbs
Desired Qualifications
- Experience across multiple therapeutic areas
- Manage complex protocols
- Take ownership of key trial activities
- Patient recruitment
- Informed consent
- Regulatory documentation
- Site audits
- Manage 2–6 trials of varying complexity
- Perform clinical procedures
- Lead study coordination from start to finish
- Work closely with investigators, sponsors, and monitors
- Mentoring junior staff
- Contributing to internal training
- Initiative
- Adaptability
- Continuous learning
- Bachelor's degree
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