Senior Clinical Trials Coordinator & Study Lead

Jobtailor; Lexington (KY); On-site; USD 52,000 - 76,000; Full time

Job summary

Jobtailor in Lexington, KY seeks a Clinical Research Coordinator to manage trials from initiation to closeout, coordinate study activities, and ensure regulatory compliance. The role requires direct collaboration with investigators, sponsors, and monitors.

Ideal candidates will bring hands-on phlebotomy, ECG, vitals collection, and strong communication skills. Knowledge of CTMS and ECRFs is essential, with a focus on timely documentation and data integrity.

Qualifications

• Hands-on experience in vital signs, phlebotomy, ECGs, and processing lab specimens.
• Solid understanding of site operations and the drug development process.
• CRC I: 1–3 years in clinical research at a clinical investigative site.
• CRC II: 3+ years as a Clinical Research Coordinator at a clinical site.
• Strong written and verbal communication 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, and lead study coordination from start to finish.
• Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
• Be 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.

Skills

Clinical Research Coordination

Phlebotomy

ECG Conducting

CTMS Usage

ECRF Management

Tools

CTMS

ECRFs

Microsoft Office

Job description

Jobtailor in Lexington, KY seeks a Clinical Research Coordinator to manage trials from initiation to closeout, coordinate study activities, and ensure regulatory compliance. The role requires direct collaboration with investigators, sponsors, and monitors.

Ideal candidates will bring hands-on phlebotomy, ECG, vitals collection, and strong communication skills. Knowledge of CTMS and ECRFs is essential, with a focus on timely documentation and data integrity.