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Clinical Research Coordinator III (Nurse - Phase 1)

  • Toronto, ON, Canada

Full-time

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Job details

Job type
Full-time
Apply by
Education
Bachelor’s degree
Working hours
37.5 hours per week
Positions available
1
Posting language
English
Posted

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: 1

Site: Princess Margaret Cancer Centre

Department: Division of Medical Oncology and Hematology – Clinical Trials Group

Reports to: Clinical Research Manager, DMOH-CTG

Salary Range: $70,473 - $88, 101 per annum

Hours: 37.5 hours per week

Shifts: Monday - Friday

Status: Permanent Full-time

Closing Date: December 09, 2026

Position Summary

The Clinical Study and Regulatory Specialist I participates in the coordination of clinical trials from protocol activation and follow up to trial closure.

Duties

  • Monitoring and promoting the quality and integrity of data, recording clinical trial data in case report forms (CRFs), and compilation of ethics and regulatory documents.
  • The coordination and monitoring of data is performed in accordance with the trial protocol, hospital and departmental guidelines and professional standards of practice.
  • Data is assessed, compiled, recorded and submitted to pharmaceutical companies or used for internal studies.
  • All data must be complete, accurate, timely and must be in compliance with applicable ICH-GCP, FDA and US federal code and Tri-Council regulations.
  • Interpret the applicable regulations in order to ensure compliance. Quality assurance procedures are utilized to ensure high quality data is obtained.

Qualifications

  • At minimum, a Bachelor’s degree in a health or science-related discipline (required)
    • Clinical Research Graduate Certificate (preferred)
  • At least two (2) years experience in some or all of Oncology, Clinical trials, medical terminology, regulatory issues involving human subjects
  • At least one (1) year experience in the review and preparation of Health Canada and Research Ethics Board submissions, including writing informed consent forms
  • Demonstrated 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
  • Satisfactory attendance
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 70473 - CAD 88101 - yearly
More about this job

Responsibilities

Coordinate clinical trials from protocol activation through follow-up and closure, while monitoring data quality and integrity. Record, compile, and submit trial data and prepare ethics and regulatory documentation in compliance with applicable protocols, policies, and regulations.

Requirements

A bachelor’s degree in a health- or science-related discipline is required, and a Clinical Research Graduate Certificate is preferred. Candidates need at least two years of experience in relevant areas such as oncology or clinical trials, plus at least one year preparing Health Canada and Research Ethics Board submissions, including informed consent forms.

Skills

  • Clinical Trial Coordination
  • Clinical Research
  • Oncology
  • Clinical Data Management
  • Case Report Forms
  • Regulatory Submissions
  • Health Canada Submissions
  • Informed Consent Writing
  • ICH-GCP Compliance
  • FDA Regulations
  • Tri-Council Regulations
  • Quality Assurance
  • Medical Terminology
  • Data Accuracy
  • Organization

Benefits

  • Healthcare of Ontario Pension Plan
  • Transit Access
  • UHN 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

Keywords

  • Clinical Research
  • Clinical Trials
  • Oncology
  • Medical Oncology
  • Hematology
  • Protocol Activation
  • Trial Follow-Up
  • Trial Closure
  • Case Report Forms
  • Clinical Data
  • Data Quality
  • Data Integrity
  • Ethics Submissions
  • Regulatory Submissions
  • Health Canada
  • Research Ethics Board
  • Informed Consent Forms
  • ICH-GCP
  • FDA Regulations
  • Tri-Council Regulations
  • Quality Assurance
  • Medical Terminology
  • Human Subjects Research
  • Pharmaceutical Companies
  • Clinical Research Graduate Certificate

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