Research Manager

Category ResearchReq Number RES-26-00034Open Date 11/5/2026Number of Openings 1Department Bloorview Research InstituteWork type Temporary Full-TimeSalary band Band H ($53.06
- $66.31/hr)FTE 1.0Posting Close Date 11/16/2026Title : Research Manager (Autism Research Centre)Department : Bloorview Research InstituteWork Type : Temporary, Full-Time (37.5 hrs per week)Start Date : November 25, 2026Start Date : November 25, 2027Supervisor : Evdokia AnagnostouJoin us in building a world of possibility Holland Bloorview Kids Rehabilitation Hospital is Canada’s largest pediatric rehabilitation hospital. We are a top 40 Canadian research hospital that is fully affiliated with the University of Toronto, and we serve over 8,500 families annually.
Our vision is to support the most meaningful and healthy futures for all children, youth and families. Providing both inpatient and outpatient programs and services, Holland Bloorview is renowned for its expertise in partnering with clients and families to provide exceptional care and is the only organization to ever achieve 100 per cent in three successive quality surveys by Accreditation Canada.
Holland Bloorview has won numerous awards including Greater Toronto's Top Employers, Canada's Top Employers for Young People and Canada's Most Admired Corporate Cultures. We are seeking a Research Manager with experience working with in multi-site clinical trial management and research administrative tasks grant writing/reporting, budget management, and technical writing. As a Research Manager within the Bloorview Research Institute the successful candidate will be required to work alongside an interdisciplinary research team working in the field of childhood neurodevelopmental disabilities and participate in BRI related events, committees and meetings. Strong critical appraisal skills, writing skills, effective communication, interpersonal and facilitation skills as well as excellent organization, time management, and priority setting skills are critical to the success of this position. Within this role the Research Manager will have the opportunity to work within multiple research labs, with different scientists and investigators whose research is focused on children and youth with neurodevelopmental disorders.
Research management at the Sponsor site for a multi-site clinical trial, from site start-up to close out. Critical skills will include effective time management, organizational skills, and experience in implementing quality assuranceEnsure research is conducted in compliance with the Tri-Council Policy Statement, Good Clinical Practice, and Health Canada regulations and policies governing clinical research (e.
TCPS-2, ICH GCP, Health Canada & FDA)Manage studies, including training, monitoring and ongoing communications with other sites and organizing meetingsEnsure quality, integrity and security on all study related information and dataDevelop policies and procedures related to the research program, ensuring external regulations and guidelines are followedDevelop, manage and forecast budgetsDevelop and monitor timelines, balancing the demands of multiple sites and monitoring recruitmentOversee study contractsCollaborate with PI regarding grant applications, new research proposals, report preparation, presentations, manuscripts and development and review of study protocolsContribute to the preparation of required reports and knowledge translation projects (e.
G. presentations, manuscripts, stakeholder progress reports, conference publications)Liaise with regulatory agencies and key project stakeholdersOversee purchases and maintenance of all research equipmentProvide day-to-day leadership, supervision, and mentorship to the clinical trials team; take leadership in problem solving regulatory and institutional processes issues with the local teamFoster a collaborative and inclusive team environment through coaching, conflict resolution, and effective communication, to assure a thriving teamMINIMUM KNOWLEDGE, SKILLS & ABILITIES A Master's degree in a health-related field or Bachelor's degree with equivalent experience. A certificate in clinical research, regulatory affairs, or project management would be an asset. SOCRA or ACRP certification preferredAt least three years of research experience requiredAdvanced knowledge of research practice, procedures, Health Canada/FDA/EMA regulations, and research ethics board applicationsDemonstrated success in developing and managing project timelines and sub-contractsDemonstrated success and understanding of managing finances and budgets for projectsDemonstrated Leadership

Skills:
Ability to take initiative and work independentlyAbility to take a leadership role as part of an interdisciplinary teamAbility to organize and facilitate the productivity of investigators and staffExceptional organizational skillsSuperior attention to detail and quality of workWorks well under pressure; Will be involved in writing papers for journals and grantsPr