About The Position
PSI is seeking an experienced freelance Senior Clinical Research Associate to support clinical research activities in Canada. The role includes onsite monitoring, site management and communication, collaboration with internal project teams and support services, feasibility research, regulatory document preparation, and participation in audits and inspections. The position offers an opportunity to develop skills, broaden therapeutic-area experience, and build expertise in clinical research.
Requirements
- College or university degree in Life Sciences, or an equivalent combination of education, training, and experience.
- Independent onsite monitoring experience.
- Experience with all types of monitoring visits in Phase II and/or III studies.
- 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.
Nice To Haves
- Experience in Oncology.
Responsibilities
- 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.
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What This Job Offers
Career Level
Senior
Education Level
Associate degree
