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

Talcura Technologies Inc.; Toronto; On-site; CAD 60,000 - 80,000; Full time

Job summary

Sunnybrook Research Institute is seeking a Full-time Research Coordinator to support ALS observational and interventional studies. The role involves coordinating regulatory submissions, patient recruitment, and all aspects of study visits, data capture, and lab logistics.

Qualifications include a Bachelor's degree and strong communication skills, with GCP/TCPS training and REDCap experience preferred. The candidate should be able to work independently and within a team on complex trials.

Qualifications

• Bachelor's degree required; graduate or professional degree an asset.
• GCP, TCSP2, NIH PHRP training preferred.
• Experience with REB and CTO documents preferred.

Responsibilities

• Conducting clinical trials in accordance with ICH GCP and TCPS guidelines.
• REB submissions, collecting and maintaining regulatory documents.
• Recruiting patients for trials and assessing eligibility with the study investigator.
• Carrying out study visits: consent, data collection, completing CRFs, maintaining source documents, scheduling follow-ups.
• Entering and maintaining data in electronic systems.
• Processing and ordering supplies for study activities.
• Processing and shipping lab specimens to central laboratory.
• Communicating with trial sponsors regarding documentation, data clarifications, monitoring visits and audits.

Skills

Interpersonal skills

Self-directed

Independent and team work

Written and verbal communication

MS Office proficiency

Data collection/management

REDCap

GCP/TCPS/NIH PHRP training

Sunnybrook experience

Education

Bachelor's degree

Graduate/professional degree (asset)

Tools

MS Office

REDCap

Job 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

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

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