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    • Minimum commitment: 15 hrs/week for 6 months (90% attendance).
    • Priority will be given to students who are able to commit to more hours, have flexible hours, and

    • Any unique skill sets that can be an asset and contribute to the growth of our clinic (ie. creative design, marketing, writing, research, IT skills, programming

    • Minimum 2-year experience in healthcare research.
    • Working closelywith the Clinical Research Lead and the study investigators, the successful candidate will

    • The Schizophrenia Division at Centre for Addiction and Mental Health (CAMH) focuses on improving the understanding, treatment, and prevention of schizophrenia

    • Experience with participatory action research, client-centered research, and/or client-oriented initiatives is desirable.
    • Leading or managing components of research projects and clinical studies.
    • Developing research ideas and designing research studies under the direction of a

    • Knowledge of clinical trials - Knowledge of clinical trial conduct in addition to skill in applying applicable clinical research regulatory requirements i.e.
    • The Cronos Clinical Science team provides scientific oversight and expertise to ensure the quality, consistency, and reliability of clinical outcome assessment

    • Reporting to the Principal Investigator and working in collaboration with a multi-disciplinary team including scientists, researchers, research staff and

    • Previous experience in the administration of neuropsychological assessments, structured diagnostic interviewing, and clinical rating scales is an asset.
    • Hold a track record in research commensurate with your level of experience post-PhD;
    • A postdoctoral research fellow position at the Hospital for Sick Children (

    • Candidates should have no more than four years of cumulative research experience following completion of the PhD.
    • Approximately 3+ years of clinical operations, clinical project associate, or equivalent clinical research experience.
    • At least 7 years of clinical research experience in the pharmaceutical industry (Strong monitoring experience is a plus).
    • Attend Clinical Meetings and Study Me.
    • Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes