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Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-Time 2026-18863 (2026-18863)
- Toronto, ON, Canada
Full-time
This opening has closed.
The original listing is kept below for reference.
Job details
- Job type
- Full-time
- Closing date
- Education
- Bachelor’s degree
- Posting language
- English
- Posted
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Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
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
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.
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.
- 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.
More about this job
Responsibilities
Coordinate observational and interventional ALS clinical studies, including patient recruitment, eligibility assessment, informed consent, study visits, data collection, and follow-up scheduling. Maintain regulatory and study records, manage data and laboratory specimens, order supplies, and communicate with sponsors about documentation, data clarifications, monitoring, and audits.
Requirements
A bachelor’s degree is required; a graduate or professional degree is an asset. The role calls for strong interpersonal and communication skills, the ability to work independently and collaboratively, and proficiency with Microsoft Office and computerized databases; clinical research experience and relevant training are preferred.
Skills
- Clinical Trial Coordination
- Good Clinical Practice
- Patient Recruitment
- Eligibility Assessment
- Informed Consent
- Clinical Data Collection
- Case Report Forms
- Source Document Management
- Electronic Data Entry
- Laboratory Specimen Processing
- Sponsor Communication
- Regulatory Documentation
- Microsoft Office
- REDCap
- Written and Verbal Communication
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
- Administrative
Keywords
- Amyotrophic Lateral Sclerosis
- ALS
- Clinical Research
- Clinical Trials
- Observational Studies
- Interventional Studies
- ICH GCP
- TCPS 2
- NIH PHRP
- Research Ethics Board
- Clinical Trials Ontario
- Patient Recruitment
- Informed Consent
- Eligibility Criteria
- Case Report Forms
- Electronic Data Capture
- Source Documents
- Regulatory Documents
- REDCap
- Microsoft Office
- Data Collection
- Data Management
- Laboratory Specimens
- Central Laboratory
- Sponsor Monitoring
- Audit Processes