Senior Clinical Research Associate
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About the role
Remote Senior Clinical Research Associate role with PSI, based in Calgary, involving on-site monitoring visits, CRF and source document review, query resolution, site management, regulatory support, feasibility work, and audit preparation. Requires a Life Sciences college/university degree or equivalent education, training and experience; independent Phase II/III monitoring experience; English and French proficiency; MS Office skills; travel ability; and a valid driver’s license. Oncology experience is a plus.
Key requirements
- • College/University degree in Life Sciences or an equivalent combination of education, training & experience
- • Required skills: Independent on-site monitoring, Monitoring visits in Phase II and/or III, CRF review, Source document verification, Query resolution, Site communication and management, Clinical study progress communication, Feasibility research, Regulatory document preparation for study submissions, Audit and inspection preparation, MS Office applications, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel
- • Required languages: English, French
- • Professional registration/licence (Canada)
Opportunity details
- • Workplace: Remote
- • Posted: Nov 10, 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: Calgary, AB, Canada
Employment type: Full-time
Compensation: CAD 120000 - CAD 150000 - yearly
Workplace type: Remote
Company Description
PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
You will:
- 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 and French is essential.
- 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.
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Nov 15, 2026