Clinical Research Coordinator — On-site Trials in Obesity Care

Speedrun Talent Network; Schaumburg (IL); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Onsite opportunity

Medical, dental, and vision insurance

401K retirement plan with companymatch

Up to 20 days PTO + holidays

Up to 14 weeks parental leave

Job summary

knownwell, Inc. is seeking a Clinical Research Coordinator (CRC) in Schaumburg, IL to oversee and coordinate all aspects of clinical trials, ensuring adherence to GCP and regulatory requirements.

The CRC serves as the primary liaison among study teams, patients, and sponsors to ensure timely study execution. Ideal candidates have a Bachelor's degree in life sciences or nursing, 3+ years in clinical research, and certifications (GCP, BLS, IATA, CSSR).

Qualifications

• Bachelor's degree in life sciences, nursing or healthcare.
• CCRC certification or willingness to obtain.
• 3+ years in clinical research; 2+ years independent trial management.
• Solid understanding of FDA, ICH GCP guidelines.
• Proficiency with data management systems and regulatory documents.

Responsibilities

• Coordinate and manage all aspects of clinical trials, including patient recruitment, screening, and enrollment.
• Schedule and oversee patient visits per study protocol.
• Oversee site initiation, monitoring, and closeout activities; calibrate equipment as needed.
• Maintain study documentation (CRFs, consents, records).
• Review monitoring follow-up letters for timely resolution of issues.
• Ensure adverse events and serious adverse events are reported.
• Manage receipt, shipment, and storage of study drug and samples.
• Handle and store study materials and biological samples properly.
• Generate invoices for study sponsors as applicable.

Skills

Phlebotomy

Organization

Leadership

Communication

Independence

Teamwork

Adaptability

Education

Bachelor's degree in life sciences/nursing/healthcare

CCRC Certification

Master’s degree preferred

Tools

CTMS/EDC systems

Regulatory documentation software

Job description

knownwell, Inc. is seeking a Clinical Research Coordinator (CRC) in Schaumburg, IL to oversee and coordinate all aspects of clinical trials, ensuring adherence to GCP and regulatory requirements.

The CRC serves as the primary liaison among study teams, patients, and sponsors to ensure timely study execution. Ideal candidates have a Bachelor's degree in life sciences or nursing, 3+ years in clinical research, and certifications (GCP, BLS, IATA, CSSR).