Position Title:Research Coordinator I
Immediate Supervisor:Dr. Jennifer Phillips
Research area:Clinical neuroscience, Mood Disorders, Suicide Prevention
Reporting Supervisor: Director Clinical Research Administration, IMHR
Start date:July 2025
Contract:Temporary, Full-time (1.0FTE or 37.5h/week), 1 year contract with possibility for renewal
Summary of Responsibilities:
The Research Coordinator 1 (RC) facilitate the conduct of clinical research under the general direction of the Supervisor/Principal Investigator (PI). The RC will assist the PI and hold supervisory responsibilities for other research staff. The RC will primarily coordinate and manage the day-to-day site operations of a multi-centre longitudinal research study in youth and adolescents with multiple mental health conditions. This project aims to provide a deeper understanding of the trajectories of youth seeking mental health care as they navigate key transition points in their development. This goal will be achieved by including sampling from a diverse range of clinical services, standardized data collection and deep phenotyping of select clinical cohorts of youth (aged 11-25 years) and will support modular clinical trials.
The RC will support the study team to ensure effective study coordination over the course of this research study, as well as participate in coordination in other research studies as needed. The RC will assist with a number of research responsibilities, including the coordination of day-to-day operations, recruiting and screening study participants, scheduling participant visits, administering structured diagnostic interviews and clinical scales, collecting neuroimaging and biomarker data, maintaining participant records, data entry/management and database maintenance, and preparing data for progress reports, research grant applications, presentations, and peer-reviewed research papers. The RC will also support and facilitate the training of other staff and research trainees on study procedures. Other administrative duties including, but not limited to, preparing Research Ethics Board (REB) submissions, participating in study-related meetings, developing and harmonizing standard operating procedures (SOPs), assisting with contracts and finances, and maintaining study documents. You will support a healthy workplace that embraces diversity, encourages teamwork and complies with all applicable IMHR policies, as well as all regulatory requirements. This position is in-person located at 1141 Carling Ave (The Royal Ottawa Mental Health Centre).
Major Responsibilities:
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