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Clinical Research Study Assistant

  • 200 Elizabeth Street, Toronto, ON, M5G 2C4, Canada

Contract

This opening has closed.

The original listing is kept below for reference.

Job details

Job type
Contract
Closing date
Working hours
37.5 Hours/Week
Positions available
1
Posting language
English
Posted

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Original job description

Archived listing. The details below describe a past opening.

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: 1
New or Replacement Position: New
Site: Toronto General Hospital
Department: Cardiology
Reports to:  Principal Investigator
Hours: 37.5 Hours/Week
Wage Range: $27.56 to $34.45 per hour
Shifts: Days
Status: Temporary Full-Time (1-year contract)
Closing Date: October 8, 2026

Position Summary

The Clinical Research Study Assistant will support clinical research studies evaluating autonomic function and non-invasive neuromodulation in patients with cardiac arrhythmias and autonomic disorders. Working under the supervision of the Principal Investigator and research team, the incumbent will assist in study coordination, participant interaction, data collection, and regulatory compliance and will perform study-specific procedures including venipuncture/phlebotomy, processing of research blood samples, and electrocardiographic (ECG) recordings in accordance with approved study protocols, UHN policies, and Good Clinical Practice (GCP) guidelines

Duties

  • Assist with screening and recruitment of study participants
  • Schedule study visits and maintain participant communication
  • Support informed consent process under supervision
  • Perform venipuncture/phlebotomy for collection of research blood samples in accordance with approved study protocols and UHN requirements
  • Assist with processing, labelling, storage, and preparation of research blood samples/specimens according to established study procedures
  • Acquire high-quality resting ECG recordings (approximately 5–10 minutes) according to standardized research protocols for subsequent heart-rate variability (HRV), P-wave alternans, and other ECG-based analyses
  • Measure and document vital signs and other study-specific physiological measurements, as required
  • Collect study data (questionnaires, vitals, device logs, diaries)
  • Maintain accurate source documentation and case report forms
  • Assist with REB submissions and regulatory documentation
  • Track and document adverse events and protocol deviations
  • Manage study files and maintain data confidentiality
  • Coordinate with clinical staff and research team members

Qualifications

  • Community college diploma in a health-related discipline, or equivalent
  • 3–6 months of related experience; clinical research experience preferred
  • Previous training and demonstrated competency in venipuncture/phlebotomy required; experience performing phlebotomy in a clinical or research setting strongly preferred
  • Experience performing ECG acquisition and obtaining high-quality ECG recordings is strongly preferred; training in study-specific ECG acquisition protocols will be provided as required
  • Experience with processing, handling, and storage of biological specimens is an asset
  • Knowledge of Good Clinical Practice (GCP) and research ethics is an asset
  • Strong organizational and time management skills
  • Excellent verbal and written communication skills
  • Ability to interact professionally and sensitively with research participants
  • Ability to follow detailed study protocols and perform standardized research procedures accurately and consistently
  • Ability to work independently and in a multidisciplinary team
  • Proficiency in Microsoft Office (Word, Excel, Outlook)
  • Experience with REDCap or clinical databases is an asset
  • The successful candidate will be required to complete applicable UHN training and competency requirements before independently performing study-specific procedures.

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
  • More about this job

    Responsibilities

    Support clinical studies of autonomic function and non-invasive neuromodulation by coordinating participant screening, recruitment, visits, communication, and data collection. Perform protocol-specific procedures, including phlebotomy, blood specimen processing, ECG recordings, and physiological measurements, while maintaining study documentation and regulatory compliance.

    Requirements

    A community college diploma in a health-related discipline or equivalent and 3–6 months of related experience are required; demonstrated venipuncture or phlebotomy competency is also required. Strongly preferred qualifications include clinical or research phlebotomy and ECG acquisition experience, alongside organizational, communication, participant-interaction, and protocol-following skills; GCP, research ethics, specimen handling, and REDCap experience are assets.

    Skills

    • Venipuncture
    • Phlebotomy
    • ECG Acquisition
    • Blood Sample Processing
    • Clinical Research Coordination
    • Participant Recruitment
    • Informed Consent
    • Data Collection
    • Regulatory Documentation
    • Good Clinical Practice
    • Research Ethics
    • Source Documentation
    • Case Report Forms
    • Vital Signs Measurement
    • Microsoft Office
    • REDCap

    Benefits

    • Healthcare of Ontario Pension Plan
    • Transit Access
    • Shuttle Service
    • Flexible Work Environment
    • Professional Development Opportunities
    • Promotion Opportunities
    • Corporate Discounts
    • On-Site Gyms

    Visa sponsorship

    Not detected in the job text

    Categories

    • Healthcare
    • Science & Research
    • Administrative

    Keywords

    • Clinical Research
    • Autonomic Function
    • Non-Invasive Neuromodulation
    • Cardiac Arrhythmias
    • Autonomic Disorders
    • Study Coordination
    • Participant Screening
    • Participant Recruitment
    • Informed Consent
    • Venipuncture
    • Phlebotomy
    • Research Blood Samples
    • Biological Specimens
    • ECG
    • Heart-Rate Variability
    • P-Wave Alternans
    • Vital Signs
    • Study Protocols
    • Source Documentation
    • Case Report Forms
    • Regulatory Documentation
    • Adverse Events
    • Protocol Deviations
    • Good Clinical Practice
    • Microsoft Office
    • REDCap
    • Data Confidentiality

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