Senior Clinical Research Associate
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About the role
Freelance Senior Clinical Research Associate role supporting clinical research activities in Canada. Responsibilities include onsite monitoring visits, CRF and source-data review, query resolution, site and vendor management, feasibility work, regulatory submissions, and audit or inspection support. A College/University degree in Life Sciences or an equivalent combination of education, training and experience is required, along with independent monitoring experience, Phase II/III visit experience, English proficiency, travel ability and a valid driver’s license. Oncology experience is a plus. Visa sponsorship is unavailable.
Key requirements
- • College/University degree in Life Sciences or an equivalent combination of education, training & experience
- • Required skills: Independent on-site monitoring, SIV, RMV and COV monitoring visits, CRF review, Source document verification, Query resolution, Site communication and management, Vendor and in-house support coordination, Study progress communication, Feasibility research, Regulatory submission support, Audit and inspection preparation and participation, MS Office applications, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel, Valid driver's license
- • Required language: English
- • Professional registration/licence (Canada)
- • Work authorization for Canada is required
Opportunity details
- • Workplace: Remote
- • Employment: Freelance
- • Posted: Oct 23, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Senior Clinical Research Associate
Location: Toronto, ON, Canada
Employment type: Full-time
Compensation: CAD 120000 - CAD 150000 - yearly
Workplace type: Remote
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
For this position, PSI is not hiring individuals who require work visa sponsorship for employment now or in the future.
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Oct 24, 2026