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Senior Clinical Research Coordinator (Contract-to-Hire)

$30 - $36 per hour

The Voluntary Protection Programs Participants' Association, Inc

We are seeking a Senior Clinical Research Coordinator to lead the execution of complex clinical trials in collaboration with Principal Investigators. This role is ideal for a seasoned coordinator ready to take on independent study management, support high‑profile trials, and mentor junior staff. You’ll ensure regulatory compliance, uphold research integrity, and protect participant safety while helping to advance cutting‑edge treatments. Candidate will handle some managerial responsibilities. Pay: $30 - $36 hourly Key Responsibilities Oversee other CRC’s while managing your own clinical trials from initiation to close‑out Independently coordinate high‑complexity and/or high‑enrollment studies Mentor and train junior CRCs and serve as a resource on assigned projects Recruit, screen, and consent study participants in compliance with protocol Dispense investigational product and monitor adherence to study requirements Collect and process biological specimens; perform vital signs, ECGs, and phlebotomy Schedule and conduct participant visits and assessments per protocol Accurately document and enter data into EDC and resolve queries per FDA guidelines Maintain regulatory binders and ensure preparedness for monitoring visits Track and report adverse events and ensure timely SAE submissions Serve as a liaison with sponsors, monitors, and referring physicians Education: Minimum Associate’s Degree (Bachelor’s preferred) Experience: 3+ years as a Clinical Research Coordinator at a research site, hospital, or private practice. Academic research experience does not qualify. Skills & Competencies In-depth knowledge of clinical research regulations, FDA guidelines and ICH‑GCP standards Phlebotomy License Strong leadership, organizational, and critical thinking skills Proficiency in CTMS and EDC systems Excellent verbal and written communication Detail‑oriented, with an unwavering commitment to data accuracy, patient safety and regulatory compliance Benefits 401(k) PTO Performance based Bonuses Dental and Health Insurance Monthly Lunch Stipend Logistics reimbursement Job Type: Full‑time Location Chicago, IL 60621 (Preferred) We are dedicated to improving patient lives through ethical, high‑quality clinical research. As a Senior Clinical Research Coordinator, you’ll help advance innovative clinical research while building your leadership career in an organization dedicated to promoting from within. Eagle Clinical Research is an equal opportunity employer. #J-18808-Ljbffr The Voluntary Protection Programs Participants' Association, Inc

Vacancy posted 4 days ago
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