Support clinical research project coordination in Waterloo with strong documentation, communication, and organizational skills. This full-time role follows Monday to Friday, 9:00 a.m. to 5:00 p.m.

Probity Medical Research seeks a Project Management Assistant supporting clinical research studies. You will coordinate site communications, regulatory documentation, project schedules, and administrative workflows. The position connects research sites, sponsors, and internal teams while supporting audits, deviations, and sponsor queries.

Key Responsibilities:

- Communicate milestones, issues, study status, and progress updates
- Serve as primary contact for sites and sponsors
- Coordinate regulatory documents, approvals, and site start-up tasks
- Maintain Portico libraries and Study Management Forms
- Support audits,



monitor queries, and protocol deviation reporting

Requirements:

- Degree or diploma in Health or Life Sciences, Business Administration, or related field
- One to two years of relevant coordination or administrative experience
- Familiarity with clinical research processes and regulatory documentation
- Solid Microsoft Word, Excel, and Outlook proficiency
- Ability to manage priorities and deadlines independently

Apply clinical research coordination, regulatory documentation, and stakeholder communication skills as a Project Management Assistant at PMR.

📌 Clinical Research Project Assistant (Canada)
🏢 Probity Medical Research
📍 Canada