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Added 11 mins ago
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Full-time
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University Health Network

Clinical Research Study Assistant - PK Team

610 University Avenue, Toronto, ON, M5G 2M9, Canada

Job type: Full-time
Apply by: Oct 9, 2026
Working hours: 37.5 Hours per week
Positions available: 2
Posting language: English
Posted: Sep 23, 2026

Apply About employer

Applications open in a new tab.

Original job description

Company Description

UHN is Canada’s #1 hospital and the world’s #1 publicly funded hospital. With 10 sites and more than 44,000 TeamUHN members, UHN consists of Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute, The Michener Institute of Education and West Park Healthcare Centre. As Canada's top research hospital, the scope of biomedical research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care. UHN has the largest hospital-based research program in Canada, with major research in neurosciences, cardiology, transplantation, oncology, surgical innovation, infectious diseases, genomic medicine and rehabilitation medicine. UHN is a research hospital affiliated with the University of Toronto.

UHN’s vision is to build A Healthier World and it’s only because of the talented and dedicated people who work here that we are continually bringing that vision closer to reality.

www.uhn.ca

Job Description

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

Qualifications

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

Additional Information

Why join UHN?
In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of benefits, programs and perks. It is the comprehensiveness of these offerings that makes it a differentiating factor, allowing you to find value where it matters most to you, now and throughout your career at UHN.

Competitive offer packages
Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP https://hoopp.com/)
Close access to Transit and UHN shuttle service
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.)

Current UHN employees must have successfully completed their probationary period, have a good employee record along with satisfactory attendance in accordance with UHN's attendance management program, to be eligible for consideration.

All applications must be submitted before the posting close date.

UHN uses email to communicate with selected candidates. Please ensure you check your email regularly. At University Health Network (UHN), artificial intelligence technologies may be used to assist in the screening, assessment, and selection of candidates for this position.

Please be advised that a Criminal Record Check may be required of the successful candidate. Should it be determined that any information provided by a candidate be misleading, inaccurate or incorrect, UHN reserves the right to discontinue with the consideration of their application.

UHN is an equal opportunity employer committed to an inclusive recruitment process and workplace. Requests for accommodation can be made at any stage of the recruitment process. Applicants need to make their requirements known.

We thank all applicants for their interest, however, only those selected for further consideration will be contacted.

Department: Research

Compensation: CAD 53747 - CAD 67184 - yearly

Apply About employer

More about this job

Responsibilities

The Clinical Research Study Assistant will perform clinical procedures such as venipuncture, vital signs, and ECGs while coordinating timed blood sampling for cancer research. They are also responsible for managing biospecimen collection kits and maintaining accurate patient documentation within the electronic medical record system.

Requirements

Candidates must have at least a community college diploma in a health-related discipline and 3-6 months of related experience. Proficiency in MS Office and strong organizational skills are required, with experience in oncology or clinical trials considered an asset.

Skills

Venipuncture
Vital signs assessment
ECG procedures
Clinical trial coordination
Biospecimen management
Patient documentation
Electronic medical records
Epic
Quality assurance
Data management
Time management
Problem-solving
Communication
Team collaboration
MS Office

Benefits

Healthcare of Ontario Pension Plan
Flexible work environment
Corporate discounts
Travel discounts
Restaurant discounts
Parking discounts
Phone plan discounts
Auto insurance discounts
On-site gyms

Visa sponsorship

Not detected in the job text

Keywords

Clinical Research
Oncology
Venipuncture
ECG
Biospecimen Management
Epic
Electronic Medical Record
Quality Assurance
Clinical Trials
Medical Terminology
Regulatory Compliance
Patient Care
Translational Research
Data Management
Healthcare
MS Office

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