Support clinical research project coordination in Waterloo with solid 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 updatesServe as primary contact for sites and sponsorsCoordinate regulatory documents, approvals, and site start-up tasksMaintain Portico libraries and Study Management FormsSupport audits,



monitor queries, and protocol deviation reportingRequirements:Degree or diploma in Health or Life Sciences, Business Administration, or related fieldOne to two years of relevant coordination or administrative experienceFamiliarity with clinical research processes and regulatory documentationStrong Microsoft Word, Excel, and Outlook proficiencyAbility to manage priorities and deadlines independentlyApply clinical research coordination, regulatory documentation, and stakeholder communication skills as a Project Management Assistant at PMR.

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