Clinical Research Coordinator I
Princess Margaret Cancer Centre
Toronto, Ontario, CA
17h ago

University Health Network (UHN) is looking for an experienced professional to fill the key role of Clinical Research Coordinator I in our Research Department.

Transforming lives and communities through excellence in care, discovery and learning.

The University Health Network , where above all else the needs of patients come first , encompasses Toronto Rehabilitation Institute, Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre and the Michener Institute of Education at UHN.

The breadth of research, the complexity of the cases treated, and the magnitude of its educational enterprise has made UHN a national and international resource for patient care, research and education.

With a long tradition of groundbreaking firsts and a purpose of Transforming lives and communities through excellence in care, discovery and learning , the University Health Network (UHN), Canada’s largest research teaching hospital, brings together over 16,000 employees, more than 1,200 physicians, 8,000+ students, and many volunteers.

UHN is a caring, creative place where amazing people are amazing the world.

University Health Network (UHN) is a research hospital affiliated with the University of Toronto and a member of the Toronto Academic Health Science Network.

The scope of research and complexity of cases at UHN have made it a national and international source for discovery, education and patient care.

Research across UHN's five research institutes spans the full spectrum of diseases and disciplines, including cancer, cardiovascular sciences, transplantation, neural and sensory sciences, musculoskeletal health, rehabilitation sciences, and community and population health.

Find out about our purpose, values and principles here.

A Clinical Research Coordinator I position is available in the laboratory of Dr. Trevor Pugh, PhD, FACMG at the Princess Margaret Cancer Centre / University Health Network in Toronto, Canada .

Located in the MaRS Centre in the heart of the downtown Discovery District, we are an integral component of multiple translational genomics projects and platforms including the Cancer Genomics Program, Tumour Immunotherapy Program, Princess Margaret Genomics Centre, and the Translational Genomics Laboratory, a joint initiative with the Ontario Institute for Cancer Research.

Working under a Project Manager, the Clinical Research Coordinator I collaborates with the Investigators and health care team to assume responsibility for the overall coordination and management of a clinical research study.

  • Responsibilities include recruitment of study participants (e.g. identify and screen potential subjects, obtain informed consent);
  • coordination of patient visits schedules as per study protocol; execution of all aspects of study visit (e.g. questionnaires, sample collection, including processing and shipment of samples according to clinical protocol).

  • The Clinical Research Coordinator I plans, implements and coordinates aspects of data collection, source documentation and data entry per UHN policy and ICH / GCP guidelines;
  • executes study-related administrative tasks, such as collection of regulatory documents, creation of investigator study files, and ethics submissions.


  • Bachelor’s Degree in a health-related field, or equivalent
  • Knowledge and interest in cancer and / or genetics is required
  • At minimum, 3 years clinical and / or professional experience
  • Up to 1 year clinical research experience preferred
  • Experience with database maintenance and electronic patient record systems an asset
  • Knowledge of ICH / GCP guidelines, IATA shipping regulations and basic laboratory procedures an asset
  • Certification as a Clinical Research Professional is preferred
  • Excellent organizational and time management skills required
  • Excellent interpersonal, verbal, and written communication skills
  • Ability to set priorities and work independently with accuracy in a multitasking environment
  • Strong Proficiency with MS Office software, Word, Excel, Outlook
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