We are looking for a skilled Clinical Research Coordinator to manage clinical studies at our on-site facility. This role involves participant coordination, compliance checks, and data collection management. As a Clinical Research Coordinator, you will oversee every aspect of the research process while adhering strictly to Good Clinical Practice (GCP) and regulatory standards.

Your background in health or life sciences will help you work collaboratively with investigators and sponsors, ensuring the integrity of protocols and data. Key Responsibilities:

- Recruit and schedule participants for clinical research studies
- Ensure compliance with Health Canada and IRB regulations
- Collect and enter data into electronic systems accurately
- Maintain and organize study documentation and subject files
- Report adverse events in a timely manner Requirements:
- Bachelor’s degree in health sciences or nursing
- 1-3 years of clinical research experience preferred
- Phlebotomy certification required
- Solid knowledge of GCP and regulatory guidelines
- Proficiency with EDC systems and Microsoft Office Suite Bring your expertise in clinical research to support impactful studies with our team.

📌 Clinical Research Coordinator On-Site (Canada)
🏢 Search Influence
📍 Canada