Clinical Research Coordinator

ClinSurge Research; Mississauga; On-site; CAD 60,000 - 80,000; Full time

Job summary

A clinical research organization in Peel Region, Mississauga seeks a motivated Clinical Research Coordinator to manage clinical research studies. You will ensure compliance with protocols, coordinate participant activities, and maintain study documents. The ideal candidate has a Bachelor's degree in health sciences and experience in clinical research. Strong communication and organizational skills are essential for this on-site role.

Qualifications

• Minimum 1–3 years of experience in clinical research preferred.
• CCRC or CCRP certification is a plus.
• Strong knowledge of Health Canada and IRB regulations.

Responsibilities

• Coordinate and conduct all aspects of clinical research studies.
• Ensure compliance with study protocols and regulatory requirements.
• Collect and enter data accurately into EDC systems.

Skills

Organizational skills

Communication skills

Problem-solving skills

Knowledge of GCP

Proficiency with EDC systems

Education

Bachelor's degree in health sciences or related field

Tools

EDC systems (e.g., Medidata, RAVE)

Microsoft Office Suite

Job description

Overview

Position Summary :

We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies in accordance with Good Clinical Practice (GCP), institutional guidelines, and federal regulations. The CRC will work closely with investigators, sponsors, and participants to ensure the integrity of study protocols and data collection.

Responsibilities

• Coordinate and conduct all aspects of clinical research studies, including participant recruitment, consent, scheduling, and follow-up.
• Ensure compliance with study protocols and regulatory requirements (Health Canada, IRB, ICH-GCP).
• Collect and enter data accurately into electronic data capture (EDC) systems.
• Maintain study documents, including electronic regulatory binders, subject files, and case report forms.
• Monitor and report adverse events and ensure timely communication with the IRB and sponsors.
• Prepare for and participate in monitoring visits, audits, and inspections.
• Collaborate with cross-functional teams, including principal investigators, sponsors, and other research personnel.

Qualifications

• Bachelor’s degree in health sciences, life sciences, nursing, or a related field (required).
• Minimum 1–3 years of experience in clinical research (preferred).
• Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) a plus.
• Phlebotomy certification and proficiency in drawing with ability to process and ship per IATA requirements.
• Strong knowledge of GCP, Health Canada, and IRB regulations.
• Excellent organizational, communication, and problem-solving skills.
• Proficiency with EDC systems (e.g., Medidata, or RAVE) and Microsoft Office Suite.

Work Environment

• On-site in physician practice and clinical research setting.
• May require handling of biological samples and / or working with patients.