Clinical Research Lead

University Health NetworkToronto, ON
CA$78,663 - CA$98,336Onsite

About The Position

As an integral member of the Department of Anesthesia & Pain Management (DAPM) – the Anesthesia Clinical Trial Unit (ACTU) Clinical Research Lead provides clinical study coordination services to investigators within the Department of Anesthesia & Pain Management. The department supports investigators across UHN, Women’s College Hospital (WCH), and Mount Sinai Hospital (MSH).

Requirements

  • At minimum, completion of a bachelor’s degree program, or recognized equivalent in a Health or Science-related discipline.
  • Clinical 3-5 years clinical and/or professional experience, and 1-2 years supervisory experience
  • 1-2 years of experience in research contract budget management
  • Possess leadership skills and have recognized experience in these areas
  • Experience managing large randomized control trials
  • Demonstrate relevant clinical research knowledge
  • Excellent written and verbal communication skills, excellent organization, prioritization skills, good computer skills, ability to learn quickly and work independently
  • Excellent interpersonal skills
  • Ability to work under pressure and attention to detail
  • Ability to perform duties in a professional and courteous manner and produce high quality work while meeting deadlines in accordance to UHN standards
  • Ability to perform multiple concurrent tasks
  • Knowledge of applicable legislative, UHN and/or departmental policies
  • 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
  • Work in compliance with UHN Vaccination Policy

Nice To Haves

  • Certification as a Clinical Research Professional (ACRP or SOCRA)

Responsibilities

  • Develop, implement, and maintain high-quality clinical trial procedures and processes
  • Hire, train, and supervise clinical trial staff
  • Liaise with investigators, administrative staff, sponsors, and clinical trials staff and develop excellent communication strategies
  • Update the Research Director on clinical trials activities, including administrative, protocol-related, data management, quality and regulatory issues and staffing
  • Oversee the submission and approval of protocols and amendments to the institutional research ethics board and all other impacted departments
  • Oversee the monitoring and quality assurance program for ACTU
  • Provide training for and enforce standard operating procedures
  • Maintain training and proficiency of study coordinators and clinical trials staff who are responsible for the data coordination
  • Ensure fiscal responsibility from resource management to cost recovery services
  • Develop workload templates and budgets for personnel, services, and resources where required.

Benefits

  • Competitive offer packages
  • Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP)
  • 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.)
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