Clinical Research Coordinator — On-Site Trials Lead

knownwell; Schaumburg (IL); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Onsite opportunity

Medical, dental, and vision insurance

401K retirement plan with companymatch

Up to 20 days of PTO + holidays

Up to 14 weeks parental leave

Work from home stipend for remote role

Job summary

knownwell, Inc. is seeking a Clinical Research Coordinator to oversee and coordinate clinical trials at our Schaumburg, IL site.

This role focuses on patient recruitment, data collection, and regulatory compliance, with an emphasis on performing phlebotomy, EKGs, and sample handling in alignment with study protocols. The CRC will act as a liaison between the clinical team, patients, and sponsors, ensuring timely study execution and adherence to GCP guidelines.

Qualifications

• Bachelor's degree in life sciences or related field; CCRC certification preferred.
• GCP/BLS certifications are advantageous.

Responsibilities

• Coordinate and manage all aspects of clinical trials, including patient recruitment, screening, and enrollment.
• Schedule and oversee patient visits, ensuring timely data collection per protocol.
• Oversee site initiation, monitoring, and closeout activities to ensure regulatory compliance.
• Maintain study documentation and regulatory binders; ensure accurate AE/SAE reporting.

Skills

Phlebotomy

EKG

Data management

Regulatory compliance

Clinical trial coordination

Communication

Time management

Education

Bachelor's degree in life sciences or related field

CCRC Certification (or willingness to obtain)

GCP/BLS certification (preferred)

Tools

CTMS

EDC

IRB regulatory

Microsoft Office

Job description

knownwell, Inc. is seeking a Clinical Research Coordinator to oversee and coordinate clinical trials at our Schaumburg, IL site.

This role focuses on patient recruitment, data collection, and regulatory compliance, with an emphasis on performing phlebotomy, EKGs, and sample handling in alignment with study protocols. The CRC will act as a liaison between the clinical team, patients, and sponsors, ensuring timely study execution and adherence to GCP guidelines.