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

Qualifications:

Education: Minimum Associate’s Degree (Bachelor’s preferred)

Experience:

3+ years as a Clinical Research Coordinator at a research site, hospital, or private practice

Note: 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. Why Join Us?

Benefits:

401k

PTO

Performance based Bonuses

Dental and Health Insurance

Monthly Lunch Stipend

Logistics reimbursement

Why you should join us:

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.

Apply now to help shape the future of clinical research.

Eagle Clinical Research is an equal opportunity employer.

Job Type: Full-time

Pay: $30.00 - $36.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off

Application Question(s):

• Have you completed the following level of education: Associate's Degree?
• Do you have EDC systems experience?
• Are you able to work onsite in Chicago?
• Do you have experience mentoring and training junior Clinical Research Coordinators or similar staff?
• Have you held a senior lead or supervisory role in clinical research?
• Do you have hands-on Venipuncture on patients (blood draws on patients)?
• Do you have experience administering vaccines and/or intramuscular/sub-cutaneous injections?
• Do you have In-depth knowledge of clinical research regulations and ICH-GCP guidelines?
• Do you have 3 years or more experience in clinical research?

Education:

• Associate (Required)

Experience:

• Clinical Research Coordinator: 3 years (Required)

License/Certification:

• Certified Phlebotomy Technician (CPT) (Preferred)

Location:

• Chicago, IL 60621 (Preferred)

Ability to Commute:

• Chicago, IL 60621 (Required)

Work Location: In person