Clinical Research Associate
Canada (Hybrid/Field) · Full-time
Monitor clinical trial sites, ensure ICH-GCP compliance, and support high-quality data collection across assigned studies.
ApplyCareers
Join a collaborative CRO team that values scientific passion, quality, and long-term partnership with sponsors and sites.
Clinical teams
Cross-functional culture
26+ opportunities across clinical operations, data, regulatory, and quality.
Canada (Hybrid/Field) · Full-time
Monitor clinical trial sites, ensure ICH-GCP compliance, and support high-quality data collection across assigned studies.
ApplyCanada (Field) · Full-time
Lead complex site monitoring visits, mentor junior CRAs, and drive inspection-ready documentation standards.
ApplyCanada / Hybrid · Full-time
Support TMF maintenance, site correspondence, visit logistics, and day-to-day study operations.
ApplyCanada · Full-time
Own end-to-end study delivery with cross-functional teams, sponsors, and investigator sites.
ApplyCanada · Full-time
Lead multi-study portfolios, manage budgets and timelines, and serve as primary sponsor contact.
ApplyCanada · Full-time
Oversee CRA resources, monitoring strategy, and operational KPIs across active programs.
ApplyRemote / Canada · Full-time
Run country and site feasibility, enrollment modeling, and investigator outreach for new studies.
ApplyCanada · Full-time
Coordinate ethics submissions, contracts, site activation packages, and green-light readiness.
ApplyCanada / Hybrid · Full-time
Design and execute site-level recruitment tactics to meet enrollment goals on schedule.
ApplyRemote / Canada · Full-time
Lead EDC build and data cleaning activities, preferably with Medidata Rave experience, through database lock.
ApplyRemote / Canada · Full-time
Build eCRFs, edit checks, and custom functions; support UAT and mid-study changes.
ApplyCanada · Full-time
Own data management plans, vendor oversight, and database lock strategy for complex trials.
ApplyCanada · Full-time
Support study design, sample size, SAP development, and interpretation of clinical results.
ApplyRemote / Canada · Full-time
Develop validated ADaM/SDTM datasets, TFLs, and reproducible analysis programs.
ApplyRemote / Canada · Contract
Guide SDTM/ADaM mapping, define.xml, and submission-ready dataset packages.
ApplyRemote / Canada · Full-time
Author protocols, informed consent, CSRs, and regulatory documents to ICH standards.
ApplyCanada · Full-time
Lead complex writing programs, peer review deliverables, and mentor junior writers.
ApplyCanada · Full-time
Process SAEs, support reconciliation, and maintain safety reporting timelines.
ApplyCanada / Hybrid · Full-time
Provide medical oversight, protocol guidance, and safety signal review for assigned trials.
ApplyCanada · Full-time
Support SOP lifecycle, internal audits, CAPA tracking, and inspection readiness.
ApplyCanada (Travel) · Full-time
Conduct GCP audits of sites, vendors, and internal processes with clear CAPA follow-up.
ApplyCanada / Hybrid · Full-time
Manage GCP training curricula, competency tracking, and compliance documentation.
ApplyCanada · Full-time
Support CTA/IND strategies, Health Canada and FDA interactions, and submission packages.
ApplyCanada · Full-time
Plan and publish electronic submissions, maintain eCTD structure, and track agency queries.
ApplyCanada / Remote · Full-time
Identify sponsor opportunities, craft proposals, and grow long-term CRO partnerships.
ApplyCanada · Full-time
Prepare budgets, RFPs, and MSA/CSA language aligned to study scope and risk.
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