Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-Time 2026-18863 (2026-18863)

Sunnybrook; Toronto; On-site; CAD 56,000 - 75,000; Full time

Job summary

Sunnybrook Research Institute in Toronto is seeking a Full-time Research Coordinator to support both observational and interventional ALS studies. You will manage study visits, informed consent, data collection, and regulatory documentation to ensure compliance with ICH GCP and TCPS guidelines.

The role requires a Bachelor's degree, strong communication skills, and experience with REB/CTO processes. Training in GCP, TCPS2, and NIH PHRP is preferred; Sunnybrook experience is an asset.

Qualifications

• 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, TCPS2, 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.

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.

Skills

Interpersonal skills

Independent and team work

Written and verbal communication

Clinical research

Regulatory knowledge

Education

Bachelor's degree

Graduate or professional degree (asset)

Tools

MS Office

REDCap

Job description

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.