Research Coordinator Ii Genomics Hlth Srvcs - Toronto, Canada - Unity Health Toronto

Unity Health Toronto

Verified Company

Toronto, Canada

2 weeks ago

Posted by:

Sophia Lee

beBee Recruiter

Description

The Genomics Health Services and Policy Research Group specializes in evaluating the adoption of new genomic technologies in clinical practice through a health technology assessment 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 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 II.

In this position, the individual will perform research activities involving project design and oversight, participant recruitment, qualitative interviewing, and summarizing and analyzing data.

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 stakeholders
Lead participant recruitment, data collection, and analysis 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 revisions
Oversee the ongoing collection, tabulation and analysis of study related data and ongoing review and development of study databases
Ensure appropriate regulations are adhered to in the conduct of research
Present research related information including conference presentations and written study reports where necessary
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:

Minimum Bachelor¿s Degree in Health Science field (preferably with 5 years related research experience)
Master¿s Degree preferred (with 3 years related research experience, MSc in Health Services Research preferred)
Experience conducting qualitative research 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 selfmotivation
Good personal and program time/detail management skills
Able to work independently and as part of a team