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About the Role

We are seeking a Clinical Research Coordinator I to assist with conducting clinical research on patients with aortic disease. The CRC 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 clinical trials, medical terminology, and regulatory affairs. 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.

Responsibilities

Recruit participants by identifying potential candidates, obtaining informed consent, and collecting demographic and clinical data.
Coordinate study visits and activities among study personnel.
Establish and maintain communications with internal and external collaborators including co-investigators, partners, and stakeholders on a regular basis.
Facilitate the submission of ethics applications, study amendments and renewal documents.
Liaise with legal office to initiate and develop research contracts/agreements with external agencies and institutions.
Ensure the smooth and efficient day-to-day operation of research and data collection activities.
Validate data, generate data queries, communicate regularly with team members and data collection centres, support with preparation of data sets for analysis.
Assist in the training of research staff including preparation and development of training documents.
Perform and oversee updates of study databases, manual of operations and data collection forms.
Develop and document related operating policies and procedures.

Requirements

Bachelor’s degree, or recognized equivalent, in a health or science-related discipline.
3 years clinical and/or professional experience.
Up to 1 year clinical research experience, preferred.
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, budgeting, contract review and mandatory reporting.
Excellent written and verbal communication skills, excellent interpersonal skills, excellent organization, and computer skills.
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.
A Criminal Record Check may be required of the successful candidate.
Any information provided by a candidate be misleading, inaccurate or incorrect, UHN reserves the right to discontinue with the consideration of their application.

Skills

ICH/GCP
Tri-Council Policy
Declaration of Helsinki
FDA CFR
Health Canada TPD
Clinical trials
Medical terminology
Regulatory affairs
Communication skills
Interpersonal skills
Organization skills
Computer skills
Creative skills
Problem-solving skills
Prioritization skills
Attention to detail

Location

Toronto General Hospital

Work Type

Temporary Full Time

Experience Level

3 years clinical and/or professional experience
Up to 1 year clinical research experience, preferred

Education Level

Bachelor’s degree, or recognized equivalent, in a health or science-related discipline
Certification as a Clinical Research Professional is an asset

Salary/Compensations

$37.47 to $46.84 per hour

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.)

About the Company

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.

Equal Opportunity

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.