Project Manager; SRI - Odette Cancer Centre Clinical Trials - Regular
Project Manager (SRI) – Odette Cancer Centre Clinical Trials
Join to apply for the Project Manager (SRI) – Odette Cancer Centre Clinical Trials role at Sunnybrook Research Institute
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Full‑time, weekdays, 8‑hr days, on‑site. Fully affiliated with the University of Toronto. Vacancy:
Project Manager – Odette Cancer Centre, Clinical Research – Regular Full‑time.
The Odette Cancer Center (OCC) Clinical Research program is part of Sunnybrook Research Institute’s ongoing commitment to excellence in innovative and high quality clinical research. As a key member of the leadership team, reporting to the OCC Trials Medical Director and Platform Research Director, the Project Manager works with 50+ physicians and over 60 OCC clinical research staff. The program includes 10 disease site groups:
Breast, CNS, GI, GU, Gynecology, Head & Neck, Hematology, Lung, Melanoma and Skin as well as two pan‑Canadian initiatives (Personalized My Treatment & The Canadian Cancer Clinical Trials Network).
The successful candidate will lead and manage strategic projects focused on improving clinical trial process efficiency through technology, automation, and AI.
- Project leadership: develop and oversee projects that leverage technology and AI to improve efficiency in clinical trial processes
- Strategic planning: collaborate with leadership and core group to define projects
- Process improvement: analyze existing workflows and identify opportunities for automation, AI integration and digital optimization
- Support and maintain program operations and vision in accordance with the Cancer Program & SRI directives and vision
- Support clinical research staff (Site & Core staff) in collaboration with physician disease site leads and senior management and leadership
- Provide oversight, support and mitigate errors in day‑to‑day operations in the clinical trials
- Assist and lead in development of initiatives to improve operational efficiency in the clinical trials
- Support senior management in Human Resource related activities including staffing, performance, scheduling and orientation of new hires
- Simplify complex clinical research processes and develop step‑by‑step instructions to help staff follow department process
- Assist in adopting organization‑wide research policies implemented by the Human Research Protections Program
- Provide support within the program to facilitate and track clinical research education initiatives and credentials and annual review of research staff training
- Program representative on working groups and committees
- Minimum 4 years recent related clinical research experience
- Technology and AI experience in research or operations
- Advanced knowledge of the clinical research process, regulations and trial finances
- Experience working with physicians, industry sponsors, and hospital departments an asset
- Experience guiding new projects through review, approvals and implementation
- Well‑developed interpersonal skills for working effectively within a diverse and inter‑professional environment
- Demonstrated excellent oral and written communication skills
- Established professional, courteous, approachable manner with a “can‑do” attitude
- Excellent customer service work ethic and team player
- Superior time management, organizational skills, accuracy and attention to detail
- Proven ability to multi‑task, prioritize work effectively and meet multiple deadlines
- University degree preferred
- Knowledge of the clinical research process at Sunnybrook/SRI a definite asset
- Interested candidates please apply online and complete all screening questions in the online portal.
- Last day for applications:
Until Filled
- Seniority level:
Mid‑Senior level - Employment type:
Full‑time - Job function:
Project Management and Information Technology - Industry: Hospitals and Health Care
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