Description
We are looking for a Full-time Research Coordinator as part of our ALS research team. We have a number of observational and interventional studies at various stages of operation. Our area of research is Amyotrophic Lateral Sclerosis (ALS) or Lou Gehrig's disease, which is a disease of the nervous system. ALS is progressive and irreversible.

Description
We are looking for a Full time Research Coordinator as part of our ALS research team. We have a number of observational and interventional studies at various stages of operation. Our area of research is Amyotrophic Lateral Sclerosis (ALS) or Lou Gehrig's disease, which is a disease of the nervous system. ALS is progressive and irreversible.

Responsibilities
Conducting clinical trials in accordance with ICH GCP and TCPS guidelines
REB submissions, collecting and maintaining regulatory documents.
Recruiting patients for clinical trials; assessing inclusion/exclusion criteria and determining eligibility with the study investigator.
Performing all aspects of study visits - informed consent process, all visit activities, collecting data, completing CRFs (electronic and paper), maintaining source documents, and scheduling follow-up appointments.
Entering and maintaining data in the electronic system
Processing and ordering supplies for study activities
Processing and shipping lab specimens to central laboratory
Communicating with trial sponsors with regards to study documentation, data clarifications,



monitoring visits, and audit processes.

Qualifications, Skills, And Knowledge
Bachelor's degree required; graduate or professional degree an asset
Proven interpersonal skills, self-directed, and ability to work independently and as part of a team
Excellent written and verbal communication skills
GCP, TCSP2, NIH PHRP training, and previous clinical research experience preferred
Experience with REB and CTO application and amendment documents preferred
Fully proficient in MS office, and the ability to work with computerized databases
Data collection and management experience, REDCap an asset
Sunnybrook experience preferred

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.

We thank all applicants for their interest but only candidates short-listed for interview will be contacted.

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, LGBTQ persons, and all others who may contribute to the further diversification of ideas.

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📌 Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-Time 2026-18863 (2026-18863 (Ontario)
🏢 Sunnybrook
📍 Ontario