ALS Research Coordinator: Clinical Trials & Data

Sunnybrook Health Sciences Centre

Toronto

On-site

CAD 55,000 - 75,000

Full time

7 days ago
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Job summary

Sunnybrook Research Institute is seeking a Full-time Research Coordinator to support observational and interventional ALS studies. The role covers regulatory submissions, patient recruitment, informed consent, data collection, and data entry across multiple study phases.

The ideal candidate holds a Bachelor's degree (advanced degree a plus), strong communication skills, and experience in GCP/TCPS with prior clinical research exposure. Proficiency in REDCap and MS Office is valued.

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, 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.

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, maintaining source documents, and scheduling follow-ups.
  • 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 regarding study documentation, data clarifications, monitoring visits, and audits.

Skills

Interpersonal skills
Self-directed
Team collaboration
Excellent written and verbal comms
GCP training
NIH PHRP training
Clinical research experience

Education

Bachelor's degree
Graduate or professional degree (asset)

Tools

REDCap
MS Office

Job description

Sunnybrook Research Institute is seeking a Full-time Research Coordinator to support observational and interventional ALS studies. The role covers regulatory submissions, patient recruitment, informed consent, data collection, and data entry across multiple study phases.

The ideal candidate holds a Bachelor's degree (advanced degree a plus), strong communication skills, and experience in GCP/TCPS with prior clinical research exposure. Proficiency in REDCap and MS Office is valued.

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