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Principal Investigator

True North Clinical Research -
Halifax, NS

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Détails du poste

Temps partiel
Il y a 6 jours

Profil recherché

Médecine
Certification ACLS

Description complète du poste

Principal Investigator

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

Serve as Principal Investigator for assigned clinical trials in accordance with Health Canada and FDA regulations and ICH-GCP
Provide direct medical care to research participants, including protocol-required visits, assessments, and medical decision-making
Serve as Sub-Investigator on additional trials to support other PI’s in their research responsibilities, as needed
Ensure the safety, rights, and welfare of all study participants
Maintain oversight of all trial-related medical decisions as outlined in FDA Form 1572
Supervise and support delegated research staff, ensuring appropriate training and compliance
Ensure studies are conducted in compliance with Health Canada and FDA regulations, GCP, IRB requirements, sponsor protocols, and company SOPs
Review and manage adverse events, serious adverse events, and unanticipated problems, ensuring timely and accurate reporting
Maintain familiarity with investigational products, including proper use and handling
Support patient enrollment and ensure informed consent is obtained appropriately and ethically
Maintain accurate, complete, and audit-ready study documentation and records
Disclose financial interests and comply with all regulatory and ethical requirements

Qualifications

Hold an MD or DO degree from an accredited medical school
Have an active, unrestricted medical license and are in good standing
Are comfortable providing hands-on care to research participants
Have experience in clinical research or a strong interest in serving as a Principal Investigator
Possess a solid understanding of Health Canada and FDA regulations, GCP, and clinical trial conduct (or are eager to learn)
Are collaborative, approachable, and value working as part of a multidisciplinary team
Communicate clearly and respectfully with participants, research staff, and sponsors
Take pride in delivering compassionate, patient-centered care
Are detail-oriented and committed to high-quality, compliant research
Prior experience as a Principal Investigator or Sub-Investigator (preferred)
ACLS certification (preferred)

Expected hours: 3 – 9 per week

Work Location: In person

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