Research Coordinator Iii Genomics Hlth Srvcs

4 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 permanent Research Coordinator III (RC III). This RC III will be primarily working on our Equity in Cancer Genetics study, which includes qualitative interviews and a chart review of cancer genetics clinics across Ontario. The RC III would also help run additional studies focused on qualitative interviews and randomized controlled trials. In this position, the individual will perform research activities involving project design and coordination, participant recruitment, qualitative interviewing, data collection and quantitative analysis, and patient and community engagement. Other tasks include assisting with study administration, research dissemination, designing and adhering to research protocols, and working with the study manager/investigator to carry out various aspects of conducting research.

**Duties & Responsibilities**:

- Conduct qualitative interviews with a variety of research participants, including patients, clinicians and decision makers
- Lead chart review data collection activities at multiple genetics clinics across Ontario
- Conduct quantitative analysis of chart review data and qualitative analysis of interview data
- Lead participant recruitment and data collection for designated studies
- Assist the study team in the initiation of new research and project design
- 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**:

- Master's Degree in Genetics or Health Science field (MSc in Genetic Counselling, Medical Genetics or equivalent experience with genetics health services research preferred)
- 5+ years of research experience in genetics health services preferred
- Knowledge of Ontario or Canadian genetics health services an asset
- Experience conducting qualitative research an asset
- Experience coordinating multi-site research studies and/or clinical trials an asset
- Experience conducting chart review data extraction and analysis 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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