Description
IQVIA is seeking a Bilingual Study Analyst to support the delivery of projects for clients in the pharmaceutical industry, governments, and academic centres in Canada, focusing on retrospective and prospective real-world evidence studies.
The successful candidate will work with other team members to assist the study Project Manager with services to support research sites and investigators in Canada.
Key responsibilities include:
- Contributing to the development of study-specific documents
- Supporting site selection and contracting
- Preparing IRB/Ethics Review Committee submissions and liaising with committees
- Setting up and training research sites
- Anticipating and troubleshooting recruitment issues
- Ensuring compliance with study requirements
- Collaborating with data managers, medical monitors, and other stakeholders
- Maintaining study records and files
- Participating in client meetings and providing presentations
Requirements:
- 1-2 years of experience in a clinical research setting
- Strong knowledge of research principles and practices
- Excellent communication and organizational skills
- Proficiency in Microsoft Office
- Bilingualism in French and English
Preferred qualifications:
- Experience with data analysis and longitudinal data analysis
- Knowledge of healthcare environments and industry trends
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