About The Position

Reporting directly to the Research Operations Manager, Clinical Research, CAMH is seeking a full-time, 12-month contract Research Analyst to provide support to a variety of clinical research activities across the divisions of the institution. The position will work across research at CAMH with a focus on the Hospital Medicine Division. The position will require a highly experienced qualitative and quantitative research background and the ideal candidate will be capable of conducting daily tasks with minimal supervision. Primary responsibilities will include supporting the gathering and analyzing of qualitative data, supporting creation of poster presentations, manuscript writing, and knowledge translation tasks. This role will also include involvement in regulatory submissions including but not limited to initial protocol submissions, protocol amendments, and communication with the Research Ethics Board, liaising with study investigators, and assisting in grant submissions. Additional duties may include data entry, data cleaning, assisting in the recruitment of participants, consenting and running study participants. The candidate may also be required to assist with other administrative duties as necessary. The individual will support a healthy workplace that embraces diversity, encourages teamwork and complies with all applicable CAMH policies, as well as all regulatory and legislative requirements. This position is located at 1001 Queen Street West. Through its core values of Courage, Respect and Excellence, CAMH is implementing its Strategic Plan: Connected CAMH, to transform lives, ignite innovation and discovery, revolutionize education and drive social change. CAMH is more than a hospital, it is a cause. CAMH is on a mission to change the way society thinks about and responds to mental illness. They aim to eliminate prejudice and discrimination and shape a world where mental illness is central to our healthcare system – a world where Mental Health is Health.

Requirements

  • Highly experienced qualitative and quantitative research background
  • Capable of conducting daily tasks with minimal supervision

Responsibilities

  • Gathering and analyzing qualitative data
  • Creation of poster presentations
  • Manuscript writing
  • Knowledge translation tasks
  • Regulatory submissions (initial protocol submissions, protocol amendments)
  • Communication with the Research Ethics Board
  • Liaising with study investigators
  • Assisting in grant submissions
  • Data entry
  • Data cleaning
  • Assisting in the recruitment of participants
  • Consenting and running study participants
  • Assisting with other administrative duties as necessary
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service