
Clinical Research Study Assistant
- Toronto, ON
- Temporaire
- Temps-plein
Number of Vacancies: 1
Site: Princess Margaret Cancer Centre
Department: Department of Surgical Oncology, Division of Urology
Reports to: Research Manager
Hours: 37.5 Hours per Week
Shifts: Mon - Fri
Status: Temporary Full-Time
Closing Date: September 19, 2025Position Summary:
Department of Surgical Oncology, Division of Urology at Princess Margaret Cancer Center is seeking a Clinical Research Study Assistant (CRSA). The CRSA participates and assists study team in preparing environment for conducting research activities as per protocol, including data and regulatory management, and central laboratory sample kit labelling support. The person assuming this role will not interact with study participants.Duties:
- Following established procedures & guidelines and comply with applicable regulations
- Maintaining and updating study databases
- Performs data transcription from health records and/or other sources, as per approved study protocol and REB authorized access.
- Redacting data and source documents
- Provides assistance with the maintenance & modification of electronic & paper information filing/retrieval methods, systems and/or formats
- Laboratory sample kit labelling activities.
- Any additional responsibilities assigned by Supervisor, and as required to fulfil this role within the non-interventional portfolio.
- At minimum, a completion of a Bachelor's degree program, or recognized equivalent in Health or Science Related Discipline.
- Certification as a Clinical Research Professional an asset
- At least two (2) years of experience in a research environment. Demonstrated relevant clinical research knowledge, previous experience in GU is an asset
- Previous research experience recruiting human subjects for clinical studies, preferred
- Knowledge of Research regulations and guidelines (such as ICH/GCP, Tri-Council Policy, Declaration of Helsinki, FDR, CFR and Health Canada TPD as required)
- Certification of IATA shipping regulations and knowledge in basic laboratory procedures, as required for this role, is an asset.
- Strong communication, organizational, time management and problem solving skills
- Excellent interpersonal, verbal and written communication skills
- Ability to set priorities and work independently with accuracy in a multitasking environment
- Ability to work under pressure with attention to detail
- Strong Proficiency with MS Office software, Word, Excel, Outlook
- Experience working with databases, conducting interviews and speaking with patients/ participants
- Adheres to confidentiality policy for sensitive patient data and information
- Competitive offer packages
- Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP
- A flexible work environment
- Opportunities for development and promotions within a large organization
- Additional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.)