Clinical Research Study Assistant - PK Team

Union: NON-UNION
Number of Vacancies: 2
New or Replacement Position: Replacement
Site: Princess Margaret Cancer Centre
Department: Research
Reports to: Senior Manager, CSP
Salary Range: $53,747 - $67,184 per annum
Hours: 37.5 Hours per week
Shifts: Days; Staggered Start/End Times and Weekend Work
Status: Permanent Full-Time
Closing Date: October 9, 2026
Job Summary
The University Health Network (UHN) is seeking a dedicated and detail-oriented individual to join the Correlative Studies Program as a Clinical Research Study Assistant – PK Team. The Correlative Studies Program supports advanced translational cancer research by providing comprehensive biospecimen management services, with the overarching goal of contributing to the discovery of novel cancer diagnostics and treatment strategies.
Duties
Working collaboratively with our PK nursing team, the Clinical Research Study Assistant will be responsible for a range of duties, including:
Perform venipuncture, vital signs assessments, and ECG procedures according to study protocols
Coordinate with healthcare teams to conduct timed blood sampling and assessments.
Facilitate the efficient flow of patients through various stages of the clinical trial
Order, prepare and manage biospecimen collection kits
Chart and document procedures and assessments in the patient electronic medical record (e.g., Epic)
Maintain and update study documents, databases, and equipment maintenance records
Apply quality assurance procedures to ensure accurate, complete, and high-quality data
Interpret and adhere to applicable clinical research regulations to maintain
At minimum, completion of a community college diploma in a health-related discipline, or equivalent, required
A bachelor’s degree, or recognized equivalent in a health-related discipline, is preferred
At least, 3-6-months related experience required
Experience performing venipuncture, ECG, and vital signs assessments an asset
At least one (1) year experience in some or all of oncology, clinical trials, medical terminology, regulatory issues involving human subjects, an asset
Strong communication, organizational, time management and problem-solving skills
Ability to work under pressure while maintaining attention to detail
Ability to perform multiple concurrent tasks
Demonstrated ability to work in a team environment and collaborate with others in assisting with the delivery of services
Client service oriented, with the ability to effectively work with diversity and appreciate that people with different opinions, backgrounds and characteristics bring richness to the challenge or situation at hand
Proficiency with MS Office software required
Experience with EPIC electronic medical record system, an asset
Certification for Transportation of Dangerous Goods, preferred

Employment type
Full-time

Work arrangement
No