- Montreal, Quebec, Canada
- Full-time · Mid
- 3–5 years
Responsible for supporting the design, deployment, configuration, and oversight of electronic Clinical Outcome Assessment (eCOA) solutions and Randomization and Trial Supply Management (RTSM) across global clinical studies.
Responsibilities
- Act as eCOA and RTSM subject matter expert during study start‑up, maintenance, and close‑out
- Define functional requirements and participate in the design and configuration of eCOA and RTSM solutions
- Draft and maintain system specifications, user requirements, edit checks, notifications, and reporting requirements
- Assist with the design of eCOA‑related Case Report Forms (CRFs)
- Create User Acceptance Testing (UAT) test scripts and coordinate or perform system validation testing
Requirements
- Bachelor’s degree in Life Sciences, Computer Science, Health Sciences, or related field