Research Coordinator (SRI) - Evaluative Clinical Sciences - Casual 2026-17083

Research Summary:

Dr. Catriona Buick (Principal Investigator) is seeking a Research Coordinator to provide support to the PI, including proposal and grant writing/editing, writing REB applications, data extraction and/or collection, study management and coordination, formal data analysis, and manuscript writing and editing. The Research Coordinator will work independently and alongside the PI, the study team, members of the healthcare team and work directly with participants.

Responsibilities Include:

• Provide comprehensive support to the Principal Investigator (PI) across all phases of research, including proposal and grant writing/editing, study design, REB applications, study coordination, and long‑term research planning. 
• Coordinate and manage research studies, including scheduling meetings, liaising with healthcare teams, faculty, and study personnel, and undertaking administrative tasks aligned with program goals.
• Independently conduct data collection and/or extraction in accordance with study protocols using tools such as REDCap, and maintain and monitor study databases. 
• Analyze and interpret research data, applying professional judgement and risk assessment to proactively address issues that may arise. Conduct qualitative and mixed‑methods analyses, including synthesizing and thematically analyzing interview data (with support as needed), and perform formal statistical analyses for quantitative studies. 
• Prepare and contribute to manuscripts, reports, conference presentations, and publications, including literature searches and reviews. 
• Act as a subject‑matter expert and resource to study and study team members.
• Recruit and engage research participants for current and future studies through clinics and/or phone outreach, and support participant follow‑up, including questionnaire administration via data management systems.

Eligibility Criteria

• Master’s degree, or PhD student/candidate with 2 years’ experience
• Experience working within the clinical environment and or with vulnerable populations (speaking/communication with patients).
• Experience with research coordination and managing research projects
• Experience using REDCap.  
• Strong interpersonal skills
• Strong computer skills and working knowledge of Microsoft Office applications
• Excellent organizational skills and attention to detail
• Ability to manage multiple tasks and meet deadlines
• Ability to work both independently and as part of a team
• Priority will be given to those who meet affirmative action criteria.

Please send application (Cover Letter and Résumé)

We thank all applicants for their interest but only candidates short-listed for interview will be contacted.

Sunnybrook Health Sciences Centre is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter.

Sunnybrook Health Sciences Centre is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to: visible minorities, all religions and ethnicities, persons with disabilities, LGBTQ persons, and all others who may contribute to the further diversification of ideas.