Clinical Research Physician
6 days ago
**Position Overview**
This is a **part-time, on-site position (2-3 full days per week)** with flexibility for **occasional weekend coverage** based on study needs.
Applicants **must be a physician licensed to practice medicine in Ontario** and in good standing with the **College of Physicians and Surgeons of Ontario (CPSO).**
**Key Responsibilities**
- Serve as **Principal Investigator** (or Sub-Investigator, depending on study design) ensuring compliance with **ICH-GCP**, **Health Canada Division 5**, and protocol requirements.
- Oversee all medical aspects of participant care, including:
- Eligibility assessment and review of inclusion/exclusion criteria
- Review of medical histories, concomitant medications, and adverse events
- Evaluation of clinically significant findings and laboratory results
- Provide **ongoing medical oversight** of participants during study participation.
- Collaborate closely with study coordinators, nurses, and other site staff to ensure smooth study execution.
- Maintain readiness for medical emergencies, ensuring crash carts, common medication boxes, and AEDs are appropriately maintained.
- Serve as the site’s **medical expert** in discussions with sponsors, monitors, auditors, and regulatory authorities.
- Participate in feasibility assessments for new studies and contribute to medical aspects of protocol and SOP development.
- Support training of clinical staff in medical care, participant safety, and protocol adherence.
- Maintain professional knowledge and clinical competencies related to both medicine and clinical research.
**Qualifications**
- **Doctor of Medicine (MD)** or equivalent degree, **licensed and in good standing with the CPSO** (College of Physicians and Surgeons of Ontario).
- _Applicants who are not currently licensed in Ontario will not be considered._
- Experience as an Investigator, Sub-Investigator, or treating physician in clinical trials is **strongly preferred**.
- Familiarity with **ICH-GCP** and **Health Canada Division 5** requirements (training can be provided).
- Strong communication and leadership skills with the ability to guide a multidisciplinary clinical team.
- Proficiency with **electronic data capture (EDC)** systems, **electronic medical records (EMR)**, and other clinical trial technologies.
**Why Join Nutrasource**
- Work within a **leading Canadian CRO** with a strong reputation in **nutraceutical and pharmaceutical research**.
- Collaborate with experienced research staff and contribute to **innovation in clinical evidence** for consumer health products.
- Flexible schedule (2-3 days/week) compatible with ongoing medical practice or academic work.
- Competitive remuneration and ongoing **GCP and Health Canada compliance training** provided.
**Job Type**: Part-time
Work Location: In person
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