Research Coordinator I Genomics Research

2 weeks ago


Toronto, Canada Unity Health Toronto Full time

The Genomics Health Services and Policy Research Group specializes in evaluating the adoption of new genomic technologies in clinical practice through a health services research lens. We conduct mixed methods research, such as randomized controlled trials, qualitative interview studies, and survey studies. We assess patient, clinician, and stakeholder preferences, health outcomes, equity considerations, and economic impacts of genetic testing. We partner with a wide range of genetic counsellors, clinicians, patients, laboratory scientists, health services researchers, and policy makers across Canada, the US, and Europe to develop the evidence, and inform policy and practice.

The Genomics Health Services and Policy Research Group is currently looking for a full-time temporary Research Coordinator I. The RC I would assist with a variety of studies focused on genetics health services research and health technology assessment. In this position, the individual will perform research activities involving project coordination, participant recruitment, qualitative interviewing, and chart review data collection. Other tasks include assisting with study administration and research dissemination, adhering to research protocols, and working with the study manager/investigator to carry out various aspects of conducting research.

**Duties & Responsibilities**:

- Assist with conducting qualitative interviews with a variety of research participants, including patients, clinicians and decision makers
- Perform data extraction of chart review data at multiple genetics clinics across Ontario
- Assist with participant recruitment and data collection for designated studies
- Assist the study team in the initiation of new research
- Assist the study team in the interpretation and implementation of study protocols
- Prepare REB submissions relative to the initiation and conduct of individual studies
- Design consent forms and implement REB revisions
- Ensure appropriate regulations are adhered to in the conduct of research
- Present research related information including conference presentations and written study reports where necessary
- Coordinate study-specific Steering Committee and Advisory Board
- Engage patient partners and other study team members with project updates
- Aid with communication of results to study team and clinical partners
- Prepare documentation for the research project including standard operating procedures, data analysis plans, research ethics submissions, and other documents as needed
- Perform literature reviews and abstract relevant data from the literature

**Qualifications**:

- Bachelor's Degree in Health Science or Policy field (MSc preferred) or demonstrable equivalent combination of specialized education and experience
- 2+ years of research experience (health services or health policy-related research experience preferred)
- Experience conducting qualitative research an asset
- Experience conducting chart review data extraction an asset
- Knowledge of genetics and genetics health services an asset
- Excellent attention to detail and proven ability to learn new skills
- Superior organizational skills to manage multiple projects in a timely manner and flexibility to adapt to changing workload
- Professionalism and self-motivation
- Good personal and program time/detail management skills
- Able to work independently and as part of a team



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