True North Clinical Research
Independent Contractor
Minimum Commitment: 3-9 hours/week
Work Location: Halifax, NS
The Opportunity
The Principal Investigator (PI) is responsible for the conduct and oversight of clinical research studies at the site level, with ultimate accountability for patient safety, regulatory compliance, and data integrity. This role is ideal for a physician who is passionate about advancing clinical research while maintaining a strong commitment to patient care.
The PI serves as the physician of record for assigned studies and plays a hands-on role in both clinical care and research activities. In addition to research responsibilities, this position requires direct interaction with and care of research participants. The PI works closely with research staff, clinical teams, sponsors, and investigators to ensure studies are conducted ethically, compliantly, and efficiently.
This role is well suited for a physician aiming to scale back from a full-time practice or looking for a semi-retired role.
Key Responsibilities
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Serve as Principal Investigator for assigned clinical trials in accordance with Health Canada and FDA regulations and ICH-GCP
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Provide direct medical care to research participants, including protocol-required visits, assessments, and medical decision-making
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Serve as Sub-Investigator on additional trials to support other PI’s in their research responsibilities, as needed
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Ensure the safety, rights, and welfare of all study participants
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Maintain oversight of all trial-related medical decisions as outlined in FDA Form 1572
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Supervise and support delegated research staff, ensuring appropriate training and compliance
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Ensure studies are conducted in compliance with Health Canada and FDA regulations, GCP, IRB requirements, sponsor protocols, and company SOPs
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Review and manage adverse events, serious adverse events, and unanticipated problems, ensuring timely and accurate reporting
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Maintain familiarity with investigational products, including proper use and handling
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Support patient enrollment and ensure informed consent is obtained appropriately and ethically
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Maintain accurate, complete, and audit-ready study documentation and records
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Disclose financial interests and comply with all regulatory and ethical requirements
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Hold an MD or DO degree from an accredited medical school
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Have an active, unrestricted medical license and are in good standing
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Are comfortable providing hands-on care to research participants
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Have experience in clinical research or a strong interest in serving as a Principal Investigator
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Possess a solid understanding of Health Canada and FDA regulations, GCP, and clinical trial conduct (or are eager to learn)
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Are collaborative, approachable, and value working as part of a multidisciplinary team
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Communicate clearly and respectfully with participants, research staff, and sponsors
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Take pride in delivering compassionate, patient-centered care
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Are detail-oriented and committed to high-quality, compliant research
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Prior experience as a Principal Investigator or Sub-Investigator (preferred)
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ACLS certification (preferred)
