Clinical Research Principal Investigator/Sub-Investigator

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Clinical Research of Ontario Ontario (CRON)

Clinical Research of Ontario (CRON) is a leading clinical research site in Scarborough dedicated to advancing healthcare through ethical, high-quality clinical trials. Partnering with global sponsors and CROs, CRON conducts studies across diverse therapeutic areas while prioritizing patient safety, scientific integrity, and community impact.

Position: Principal Investigator/Sub-Investigator (Clinical Research)

Position Summary

The Principal Investigator (PI) will oversee and lead clinical research studies conducted at Clinical Research of Ontario. The PI is responsible for the overall design, conduct, integrity, and management of clinical trials, ensuring adherence to Good Clinical Practice (GCP), Health Canada regulations, and institutional ethics standards. This role requires both strategic and hands-on leadership in clinical research design, patient safety oversight, and scientific communication.

Key Responsibilities

• The Principal Investigator will be responsible for confirming patient eligibility and ensuring adherence to study inclusion and exclusion criteria
• Ensure that all aspects of study conduct comply with regulatory requirements, protocol specifications, and CRON policies.
• Ensure patient safety is maintained throughout all phases of the study.
• Review and assess adverse events, serious adverse events (SAEs), and protocol deviations.
• Oversee data collection, accuracy, and reporting to ensure scientific validity and compliance with GCP.
• Supervise co-investigators, study coordinators, and research staff.
• Participate in training and continuing education of research personnel.

Qualifications & Experience

• MD (licensed in Ontario) with specialization in Internal Medicine, Family Medicine, or other specialt
• Clinicak research experience is an ASSET

Job Type: Part-time

Pay: From $150.00 per hour

Work Location: In person