Analyste d’études - Données probantes en vie réelle (Real World Evidence)/Analyste d’études - Données probantes en vie réelle (Real World Evidence) Bilingual
usd72.5k - usd120.9k per yearIQVIA
IQVIA seeks a bilingual study analyst to support real-world evidence projects across Canada, working with pharmaceutical companies, governments, and academic institutions. The role spans the full study lifecycle from design through reporting, coordinating with research centers, investigators, and internal teams on retrospective and prospective studies.
Responsibilities
- Develop study-specific documents including protocols, study plans, and data collection tools
- Support research center selection, contracting, and site initiation with training and ongoing coordination
- Prepare IRB/ethics committee submissions and manage committee communications to expedite review
- Monitor ongoing data entry, protocol compliance, and address recruitment challenges at active sites
- Coordinate safety reporting, maintain investigator site files and study master files, support site closeout
Requirements
- 1–2 years experience in clinical trial or study support at academic/hospital institution
- 1–2 years experience in clinical research or related support role
- Bilingual fluency (French and English)
- Strong organizational and communication skills
- Ability to manage multiple studies and coordinate with diverse stakeholders
- Understanding of clinical research regulations and ethics requirements
Vacancy posted 8 hours ago
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