Senior Clinical Research Associate

PSI CRO AG

Senior Clinical Research Associate conducting onsite monitoring and regulatory support for a global medical research company in Canada. Managing clinical-trial sites, CRFs, queries, audits, and study submissions.

Posted 8/14/2026full-timeRemote • Toronto • 🇨🇦 CanadaSenior💰 CA$120,000 - CA$150,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in conducting onsite monitoring visits, including SIV, RMV, and COV, while effectively managing site communication and supporting regulatory submissions. Proficient in both English and French, with strong problem-solving and collaboration skills in a dynamic team environment.

Highest-signal resume keywords

On-Site Monitoring ExperiencePhase II And III MonitoringOncology ExperienceFull Working Proficiency In English And FrenchMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

CRF ReviewSource Document VerificationQuery ResolutionFeasibility ResearchAudit PreparationInspection Participation

Soft Skills

Communication SkillsCollaboration SkillsProblem-Solving SkillsAbility To Multitask

Industry Keywords

Life SciencesRegulatory SubmissionsSite ManagementMonitoring Visits

About the role

Key responsibilities & impact

Conduct and report SIV, RMV, and COV onsite monitoring visits
Perform CRF review, source document verification, and query resolution
Manage site communication and management
Serve as a point of contact for in-house support services and vendors
Communicate with internal project teams regarding study progress
Participate in feasibility research
Support the regulatory team in preparing documents for study submissions
Prepare for and participate in audits and inspections

Requirements

What you’ll need

College/University degree in Life Sciences or equivalent combination of education, training, and experience
Independent on-site monitoring experience
Experience with all types of monitoring visits in Phase II and/or III
Experience in Oncology is a plus
Full working proficiency in English and French
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
Must not require work visa sponsorship for employment now or in the future

Benefits

Comp & perks

Remote work option
Opportunity to further develop skills
Opportunity to widen therapeutic area experience
Opportunity to become an expert in clinical research