Major Responsibilities

• Recruit eligible subjects, obtain informed consent, perform protocol specific study procedures, and complete data entry
• Co-ordination of research MRI scans with clinical visits
• Preparation of regulatory applications, research ethics board applications, amendments and notifications to Health Canada
• Maintenance of all documentation associated with assigned clinical trials
• Work with the research team to design, document and execute the clinical trial
• Other duties related to research as assigned

Education and Experience:

• Minimum of Bachelor’s Degree in health-related field or equivalent
• Attention to detail
• Recognized certification in clinical research (e.g., ACRP or SOCRA) an asset
• Demonstrated research experience in HC Division 5 clinical trials, including in-depth knowledge of ICH/GCP, PHIPA, TCPS, Health Canada and FDA regulations.
• Demonstrated proficiency in writing
• Excellent word processing and computer skills
• A thorough understanding of research ethics (i.e. informed consent process, patient recruitment), ICH GCP, PHIPA, FDA and Health Canada regulations an asset
• Excellent oral and written communication skills.
• Outstanding skills in managing inter-personal interactions.
• Strong organizational capabilities and ability to coordinate multiple projects, perform concurrent tasks, and work under pressure
• Demonstrated ability to work independently and to take initiative

In addition, the individual is expected to:

Work within the larger context of Sunnybrook Health Sciences Centre (SHSC) and observe Hospital and department rules and regulations, policies, procedures, practices, safety procedures and current legislation, in particular the Human Rights Code regarding discrimination and harassment.  Ensure the confidentiality of patient, employee, graduate student and Hospital information at all times. Work cooperatively and constructively with the other members of SHSC staff. Perform the above functions in a manner, which reflects the Hospital philosophy and mission of service, while promoting and maintaining good public relations with patients, visitors and Hospital staff.

In accordance with Canadian Employment and Immigration guidelines, applicants must be eligible to work in Canada. In accordance with Canadian immigration requirements, this advertisement is directed initially to Canadian citizens and permanent residents.

Sunnybrook Research Institute is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter.

Sunnybrook Research Institute is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to: visible minorities, all religions and ethnicities, persons with disabilities, LGBTQ2S+ persons, and all others who may contribute to the further diversification of ideas.

To apply for this position, please:

Send a cover letter and Curriculum Vitae and the names of three potential references to:

Mrs. Kimberly Allen

kimberly.allen@sunnybrook.ca

Please put “CHC Clinical Research Coordinator” in the subject line

Deadline for application: June 11^th, 2024

We thank you in advance for your interest. Only those candidates selected for an interview will be contacted. No phone calls please.

Application screening will continue until a suitable candidate is identified.