
Research Associate
- Sherbrooke, QC
- Permanent
- Full-time
- Orchestrate three multi‑stage reviews (effectiveness; barriers/facilitators; implementation strategies) and co‑develop a usable framework/toolkit with partners.
- Own the review pipeline: protocols (PRISMA‑P/PROSPERO), comprehensive database and grey‑literature searches, dual screening, structured data extraction, and risk‑of‑bias/quality appraisal (e.g., RoB 2, ROBINS‑I, JBI).
- Conduct quantitative syntheses (meta‑analysis/meta‑regression in R/Stata) and/or qualitative/realist syntheses as appropriate.
- Convene and coordinate national/international collaborators and community advisors; steward milestones and CIHR progress reporting.
- Translate evidence into impact: draft manuscripts (first/co‑first authorship opportunities), conference abstracts, policy briefs, and implementation tools (logic models, decision aids, checklists).
- Co‑design and facilitate stakeholder workshops and integrated knowledge translation activities.
- Provide methodological leadership on rapid reviews, scoping reviews, bibliometric analyses, and realist syntheses in digital health, equity‑focused interventions, and implementation‑strategy reporting/quality.
- Mentor graduate students and research assistants in rigorous, transparent, and open‑science workflows (preregistration, living reviews, reproducible scripts, data management).
- Contribute to grant writing (CIHR/FRQ/PHAC/SSHRC), ethics submissions, and data‑management plans.
- Resources: Licences for statistical and qualitative software; data storage; professional‑development funds.
- Growth: Authorship opportunities, mentorship, and exposure to a high‑performing, multi‑site research network spanning academia, public health agencies, and community partners.
- PhD (or equivalent) in public health, epidemiology, health services research, nursing, implementation science, or a related discipline.
- Peer‑reviewed publication record in systematic and/or scoping reviews.
- Proficiency with review software (e.g., Covidence/DistillerSR, RevMan/R, NVivo/Atlas.ti).
- Strong quantitative (meta‑analysis in R/Stata) and/or qualitative synthesis skills.
- Excellent scientific writing and project‑management skills.
- Eligible to work in Canada.
- Post‑doctoral training or ≥ 2 years’ post‑PhD experience in systematic reviews or knowledge translation.
- Experience with STBBI, point‑of‑care diagnostics, or harm‑reduction research.
- Familiarity with implementation frameworks (e.g., CFIR, ERIC) and reporting guidance (e.g., TIDieR, AACTT).
- Experience with GRADE, economic evaluation, complex intervention synthesis, or equity‑focused appraisal.
- French proficiency; experience engaging community or Indigenous partners.
- Cover letter (max 2 pages) outlining relevant experience and fit.
- Curriculum vitae.
- Two sample publications (preferably systematic reviews).
- Contact information for three referees (letters on request).