The Genomics Health Services and Policy Research Group specializes in evaluating the adoption of new genomic technologies in clinical practice. We conduct mixed methods research such as randomized controlled trials, qualitative, and survey studies. We assess patient & provider preferences, health outcomes, and economic impacts of implementing genetic tests in practice. We partner with a wide range of clinicians, laboratory scientists, health services researchers and policy makers across Canada, the US & Europe to develop the evidence, and inform policy and practice.
The Genomics Health Services and Policy Research Group is currently looking for a casual temporary Research Assistant I. In this position, the individual will provide essential assistance, organizational and administrative support to research projects at a basic level. Tasks may include (1) collecting and recording data through survey, chart review, and in-depth interviewing, (2) processing and analyzing data, (3) following research procedures and helping maintain protocols, standard operating procedures and REB documents, and (4) obtaining consent and conducting study visits. In general, the role provides project support for the Research team and Principal Investigator. The Research Assistant may also contribute to the funding and grant processes by providing information, helping quality check documentation, and liaising with internal and external partners.
Duties & Responsibilities
- Aiding with the collection and transcription of study-related data and/or reviewing data
- Assisting investigators in the execution of research, including helping with consenting and study visits
- Assisting investigator in the interpretation and implementation of study protocols
- Preparing REB submissions relative to the initiation and conduct of individual studies
- Assisting with revisions of consent forms and other REB-related documents
- Conducting interviews with research participants using standardized questionnaires
- Collecting data via phone calls, interviews, chart reviews and surveys
- Administration of the Letter of Information and Consent Form to study participants
- Help maintain CVs of the PI and external partners
- Ensuring appropriate regulations are adhered to in the conduct of research
- Present research related information including conference presentations and written study reports where necessary
- Engaging patient partners and other study team members with project updates
Qualifications
- Preferred Bachelor’s Degree in Health Science field (preferably with 3 years related research experience), or equivalent level of relevant experience
- Excellent attention to detail and proven ability to learn new skills.
- Superior organizational skills to manage multiple tasks 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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Thank you for applying.
