
Manager, Research Ethics Board
- Toronto, ON
- Permanent
- Temps-plein
Hours of Work: Day shifts from Monday to Friday (some evening and weekend hours may be required based on operational needs) - subject to change as per Management RightsLocation: Humber River Health, Wilson Site
Employee Group: Management
Reporting Relationship: Vice President, Research & InnovationOVERVIEW OF ROLEThe Research Ethics Board (REB) is responsible for the ethical assessment and approval of all research involving human subjects at Humber River Health (HRH) with a mandate to approve, reject, propose modifications to, or terminate proposed or ongoing research in accordance with hospital policies, national guidance documents and legal requirements. This role will manage research ethics at HRH through the Research Ethics Office.RESPONSIBILITIESREB Operations & Administration:
- Manage and assess research proposal submissions through all stages of the approval process
- Maintain compliance with the Tri-Council Policy Statement (TCPS2), Health Canada Division 5, ICH-GCP, and relevant provincial and institutional guidelines.
- Manage REB meetings: schedule, set agendas, ensure quorum, prepare minutes, and communicate decisions.
- Assess submitted proposals to determine required review process (delegated vs full board).
- Review delegated proposal submissions in consultation with the Chair of Research Ethics and identify issues and revisions to be made.
- Administer appeals process for rejected proposals via the Toronto Academic Health Science Network (TAHSN) REB Appeals Process.
- Develop and lead the implementation of structural and operational changes to increase efficiencies and adapt to constantly evolving standards to augment governance best practices, oversight, and compliance.
- Develop collaborations with other REBs to increase efficiencies and streamline research ethics review for multi-site studies.
- Administer and maintain the Online Research Ethics Review System (HRH eREB system), ensuring smooth operation and timely escalation of issues as needed.
- Act as a resource and provide guidance for research ethics policies and procedures and regulatory guidelines (U.S. and Canadian) for Research Ethics Board members, researchers, clinician-scientists, research support staff, administrative staff, clinical leadership teams, and external stakeholders (e.g., pharmaceutical representatives, external physician investigators).
- Provide general administrative support to the Chair of Research Ethics and the REB.
- Recruit, orient, and train REB members and staff, including community representatives and experts.
- Organize REB meetings and ensure quorum, documentation, and efficient decision-making.
- Support Research strategic initiatives as needed.
- Interpret and apply evolving national and international research ethics and regulatory policies.
- Ensure REB decisions are well documented and issued in a timely, transparent, and consistent manner.
- Prepare the REB for audits or inspections by Health Canada, the institution, or affiliated academic bodies.
- Develop, implement, and update institutional REB policies and SOPs.
- Monitor and interpret changes to relevant laws, guidelines, and standards.
- Ensure compliance with TCPS2, Health Canada, FDA (if applicable) and institutional policies.
- Serve as the primary point of contact for investigators and research staff on ethics-related matters.
- Provide guidance on REB submissions, informed consent, and protocol development.
- Develop training materials and workshops to promote ethical research conduct.
- Promote awareness of ethical issues in research.
- Provide continuing education on ethics and regulatory updates to REB Members.
- Act as an advisory to the research community internally and externally.
- Bachelor’s Degree in Health Sciences, Public Health, Bioethics and/or related discipline required. Graduate degree in Health Science, Ethics or related discipline preferred
- Member of Canadian Association of Research Ethics Boards (CAREB-ACCER) preferred
- 5 years of experience in research ethics required, preferably experience in managing or supporting REBs within a healthcare or academic setting
- MS Office (Outlook, Word, Excel, PowerPoint, etc.) proficiency, required
- Knowledge and applied experience in research best practices, Canadian healthcare system and healthcare funding landscape, and experience in executing research studies in hospital settings
- Collaborative, interpersonal, creative, committed to research integrity, leadership, diplomacy behavioural style
- Relationship building with participants, principal investigators, all levels of management and leadership staff, physician and all stakeholders involved in the research process.
- Good Clinical Practice (GCP) training, preferred
- Research methods training (e.g., quantitative, qualitative, research design, etc.) and knowledge on pharmaceutical research regulations and guidelines, preferred