Clinical Research Coordinator I

Posted 6 Days Ago
Be an Early Applicant
Toronto, ON, CAN
In-Office
Entry level
Healthtech • Biotech • Pharmaceutical
The Role
Coordinate and manage multiple home dialysis clinical studies through screening, recruitment, informed consent, study visits, sample collection/processing, data management, safety monitoring, REB submissions, audits, and regulatory compliance (ICH-GCP, Tri-Council, PHIPA, Health Canada/FDA). Support feasibility reviews, budgeting, contracts, and develop tools to ensure data integrity while working with minimal supervision.
Summary Generated by Built In
Job Description

The Department of Nephrology requires a Clinical Research Coordinator I to work in clinical research in the Home Dialysis program.  This position is an integral part of the Home Hemodialysis program and will coordinate several studies initiated by University Health Network and external sponsors through all phases of the research.  The role will include promotion of research within the program.

 

Duties:

  • Coordinate several clinical studies, including screening, recruitment, obtaining informed consent, execution of all aspects of study visits and assessments, sample collection and processing, data management, monitoring of safety, maintenance of research assets
  • Assist with study audits and monitoring
  • Conduct studies ensuring support of patients with chronic disease and in compliance with ICH-GCP, Tri-Council Guidelines, PHIPA, Health Canada/FDA regulations, UHN policies
  • Contribute to the review of studies to determine feasibility
  • Submission of studies for review by REB both at UHN and CTO
  • Apply knowledge of investigator/sponsor-initiated research process, budgeting, and contract reviews
  • Develop tools to ensure accurate data collection and data integrity
  • Exercise independent judgement and decision making
  • Work with minimal direction from leadership
  • May provide leadership within the team
  • Participate in projects as required

Additional Information

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.

Skills Required

  • Coordinate clinical studies including screening, recruitment, informed consent, study visits, and assessments
  • Sample collection, processing, and maintenance of research assets
  • Data management and ensuring data integrity
  • Knowledge of ICH-GCP, Tri-Council Guidelines, PHIPA, Health Canada/FDA regulations, and UHN policies
  • Experience with REB submissions and review processes (UHN and CTO)
  • Assist with study audits and monitoring
  • Familiarity with investigator/sponsor-initiated research processes, budgeting, and contract review
  • Ability to exercise independent judgment and work with minimal direction
  • Ability to support patients with chronic disease and promote research within the program
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The Company
HQ: Toronto
24,490 Employees
Year Founded: 1986

What We Do

University Health Network is Canada's largest research hospital and a public research and teaching hospital network in Toronto, Ontario, known for its scope of research and complexity of cases.

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