Clinical Research Coordinator III (Nurse)

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. Job Description We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada: Conduct and report SIV, RMV, COV onsite monitoring visits Perform CRF review, source document verification and query resolution Be responsible for site communication and management Be a point of contact for in-house support services and vendors Communicate with internal project teams regarding study progress Participate in feasibility research Support regulatory team in preparing documents for study submissions Prepare and particiapte on audits and inspections Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience Independent on-site monitoring experience Experience in all types of monitoring visits in Phase II and/or III Experience in Oncology is a plus Full working proficiency in English. Proficiency in MS Office applications Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel Valid driver’s license Additional Information This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research. Compensation: CAD 120000 - CAD 150000 - yearly

The role involves conducting and reporting on various onsite monitoring visits, including SIV, RMV, and COV. The coordinator is responsible for site communication, CRF review, and supporting regulatory submissions and audits.

Candidates must have a degree in Life Sciences and independent experience in Phase II and/or III monitoring visits. Proficiency in English, MS Office, and a valid driver's license are required, with oncology experience being a plus.

• Problem solvingPreferred

Identified from the job description. Confirm important requirements above.

• On-site Monitoring
• CRF Review
• Source Document Verification
• Query Resolution
• Site Management
• Feasibility Research
• Regulatory Documentation
• Audit Preparation
• Oncology
• MS Office
• Problem Solving
• Collaboration
• Multitasking

• Science & Research
• Healthcare

Minimum education

Bachelor’s degree

Minimum experience

5+ years

Apply by

Sep 10, 2026

Posting language

English

Working hours

40 hours per week

Seniority

Mid-Senior level