Location

Estimated commute

Job address

304 Victoria Avenue North, Hamilton, ON L8L 5G4

 

Benefits

Pulled from the full job description

• Paid time off
• On-site parking

 

Full job description

Job Summary

Premier Clinical Trial Network (PCTN) is a growing multi-specialty clinical research organization conducting Phase II–IV industry-sponsored clinical trials. We partner with leading pharmaceutical and biotechnology companies to deliver high-quality clinical research while maintaining the highest standards of patient care, regulatory compliance, and Good Clinical Practice (ICH-GCP).

We are seeking an experienced and motivated Clinical Research Coordinator (CRC) to join our expanding team.

Working under the overall direction of the Medical Director and Director of Clinical Operations and reporting to the site manager, the Clinical Research Coordinator is responsible for the day-to-day coordination and management of assigned clinical trials from study start-up through close-out.

The successful candidate will ensure compliance with study protocols, ICH-GCP guidelines, Health Canada regulations, Research Ethics Boards (REB), sponsor requirements, and PCTN Standard Operating Procedures.

Key Responsibilities

Study Coordination

• Coordinate assigned clinical trials from study start-up through close-out under the supervision of the Principal Investigator and Clinical Operations team.
• Schedule and conduct study visits in accordance with study protocols.
• Collect vital signs, ECG, and other study activities according to protocol
• Process, ship, track biological samples and maintain study supply inventory

Participant Recruitment

• Recruit, screen, consent, and enroll study participants.
• Coordinate participant visits, specimen collection, and investigational product activities.
• Promote participant retention and protocol compliance throughout the study.

Regulatory & Documentation

• Prepare and maintain study regulatory files and essential documents.
• Complete accurate source documentation and electronic data entry (EDC).
• Assist with REB submissions, protocol amendments, and study documentation.

Safety & Quality

• Document and report adverse events in accordance with study requirements.
• Support monitoring visits, audits, and regulatory inspections.
• Ensure compliance with study protocols, ICH-GCP, and site SOPs.

Collaboration

• Work collaboratively with investigators, sponsors, CROs, and research staff.
• Attend study meetings and complete required training.
• Perform other clinical research duties as assigned

Qualifications:

• Diploma or Bachelor's degree in healthcare or science discipline.
• Clinical Research Certificate, Post-Graduate Clinical Research Program, or equivalent clinical research training is strongly preferred.
• 2+ years of experience coordinating industry-sponsored clinical trials.
• Strong organizational, communication and time management skills
• Proficiency with Microsoft office and EMR
• Experience with participant recruitment, specimen processing, ECG, or investigational product management is an asset

Pay: $28.00-$32.00 per hour