
Clinical Research Coordinator I
- Toronto, ON
- Permanent
- Temps-plein
Number of vacancies: 1
Site: Toronto General Hospital
Department: Division of Respirology
Reports to: Clinical Research Manager
Hours: 35 hours per week
Shifts: Monday to Friday
Status: Permanent Full-Time
Closing Date: September 5, 2025Position Summary
We are seeking a Clinical Research Coordinator I to assist with research studies in the Toronto Lung Transplant Program (TLTP). The CRCI will apply fundamental knowledge of research principles, theories, and concepts, and be familiar with research regulations and guidelines such as ICH/GCP, Tri-Council Policy, Declaration of Helsinki, FDA CFR, and Health Canada TPD. The ideal candidate will have a strong understanding of medical terminology and regulatory issues. We are looking for an energetic, patient-oriented individual who thrives in a fast-paced clinical research environment. This role requires both research and patient-facing clinical experience.All applicants must submit a cover letter explaining why they believe they would be a valuable addition to Canada's top hospital - ranked third best in the world.Duties
- Recruitment of study participants (e.g. identifying, screening potential participants and obtaining informed consent)
- Coordinate study visits and activities and process samples
- Facilitate the submission of ethics applications, study amendments and renewal documents
- Ensure the smooth and efficient day-to-day operation of research and data collection activities
- Implementing and coordinating all aspects of data management including data collection, data entry into CRFs, and source documentation, as per UHN policy and ICH/GCP guidelines
- Participate in internal monitoring and quality assurance activities
- Bachelor's degree, or recognized equivalent, in a health or science-related discipline plus a certification in a Clinical Research Program
- At least 3 years clinical research experience
- Applies knowledge of clinical research principles and practice
- Applies knowledge of research regulations and guidelines, such as ICH/GCP guidelines, Tri-Council Policy, Declaration of Helsinki and FDA CFR and Health Canada TPD, as required
- Applies knowledge of investigator-driven research processes, contract review and mandatory reporting
- Excellent written and verbal communication skills, excellent interpersonal skills, excellent organization, and computer skills with experience using REDCap, Medrio and Medidata
- Possess creative and problem-solving skills with the ability to learn quickly and work independently
- Excellent prioritization skills with the ability to perform multiple concurrent tasks while meeting tight deadlines
- Ability to work under pressure with great attention to detail
- Ability to perform duties in a professional and courteous manner and produce high quality in accordance with UHN standards
- 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
- Certification as a Clinical Research Professional is an asset
- Competitive offer packages
- Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP
- 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.)