Research Analyst - Institute for Mental Health Policy Research

CAMHToronto, ON
CA$28 - CA$37Onsite

About The Position

CAMH is seeking a casual Research Analyst (RA) to support a clinical Non-Therapeutic Research on Cannabis (NTRC) study. This study is a randomized, double-blind human laboratory study evaluating THC self-titration in cannabis users when vaping. The RA will report to the Senior Scientists and Research Manager of the Institute of Mental Health Policy Research (IMHPR), which is a key driver in building the knowledge base for policy decisions, development of mental health interventions, and health system improvement. The RA will work closely with other Research Analysts, the Research Coordinator, Registered Nurse, and other team members to support data collection. The successful candidate will support a workplace that embraces diversity, encourages teamwork, and complies with all applicable and regulatory requirements. This position will be in-person and provide support at various CAMH sites: 250 College Street and 33 Ursula Franklin Street in Toronto. CAMH's core values are Courage, Respect, and Excellence, and they are implementing their Strategic Plan: Connected CAMH, to transform lives, ignite innovation and discovery, revolutionize education, and drive social change. CAMH aims to change the way society thinks about and responds to mental illness, eliminate prejudice and discrimination, and shape a world where mental illness is central to our healthcare system.

Requirements

  • Support a clinical Non-Therapeutic Research on Cannabis (NTRC) study
  • Work closely with other Research Analysts, Research Coordinator, Registered Nurse, and other team members
  • Support data collection
  • Support a workplace that embraces diversity, encourages teamwork, and complies with all applicable and regulatory requirements

Responsibilities

  • Recruitment
  • Pre-screening
  • Blood sample processing
  • Collecting cognitive and mood assessments
  • Conducting mental status and psychiatric screenings
  • Taking vital signs
  • Electronic data collection and documentation
  • Supporting quality assurance activities and ethics submissions
  • Ongoing support, training, and communication with other research team members
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