Junior/Intermediate Clinical Trial Associate
$60,000–$90,000 year
Hybrid · Ottawa, Ontario, Canada
Ottawa, Ontario, CanadaHybridFull Time$60,000–$90,000 yearMid LevelNot Specified
Type
Full Time
Level
Mid Level
Education
Not Specified
Job Summary
Regulatory-focused Clinical Trial Associate supports start-up and ongoing regulatory submissions for Alzheimer’s trials, coordinating regulatory documents, IRB submissions, site file maintenance, and liaising with sponsor/CRO; requires ICH-GCP knowledge, bilingual French and English, strong detail orientation, and ability to manage multiple studies in a fast-paced environment.
Required Qualifications
- Minimum of 2 years’ experience in a Regulatory Specialist role supporting a clinical site and/or sponsor organization
- Strong attention to detail and excellent organizational and communication skills
- Ability to manage multiple priorities and work effectively in a team
- Fluency in French and English (spoken and written)
- Knowledge of ICH-GCP and regional regulatory requirements (EMA, FDA, Health Canada)
- Experience with submission processes and regulatory systems (eISF)
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