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Leads strategic and operational procurement for academic, operational, and capital equipment needs. Manages sourcing initiatives, RFX processes, contract negotiations, supplier relationships, procurement governance, compliance, risk, savings tracking, and implementation. Partners with internal stakeholders and UHN teams to develop procurement strategies, manage complex cross-functional projects, prepare business cases and financial analyses, and provide recommendations to senior leadership. Ensures alignment with public procurement laws, trade agreements, and organizational policies.

Provides comprehensive administrative and operational support to the Princess Margaret Commercialization team. Responsibilities include managing calendars and meetings, maintaining Wellspring and agreement records, coordinating Innovation Accelerator activities, monitoring shared communications, supporting reception and inquiries, processing expenses, assisting with projects, and improving administrative processes. The role requires strong organization, communication, customer service, confidentiality, attention to detail, and proficiency with Microsoft Office and workflow systems.

Performs financial planning, budgeting, forecasting, reporting, reconciliation, variance analysis, and clinical financial data modeling. Prepares monthly, quarterly, and annual reports and dashboards, supports month-end close, analyzes financial and operational trends, and provides data-driven recommendations to hospital leaders. Collaborates with program managers, directors, and corporate finance teams on funding, case costing, audits, cost savings, and revenue opportunities.

The Program Development Lead supports Target 2035 through grant and award proposal development, application coordination, post-award reporting, milestone tracking, and impact measurement. The role also contributes to scientific communications, newsletters, reports, websites, outreach, trainee programs, webinars, workshops, and international stakeholder coordination. Success requires strong scientific and grant writing, research development, organizational, communication, and collaboration skills within a multidisciplinary biomedical research environment.

Manages financial planning, budgeting, performance measurement, reporting, productivity analysis, and financial systems for Chronic Kidney Disease and Ajmera Transplant Centre programs. Partners with hospital leadership to analyze financial and operational results, develop strategies, prepare reporting packages, and oversee portfolio and special projects. The role also provides administrative leadership and supervises project-related work.

Leads earned media, public relations, strategic communications, issues and crisis communications, and internal Town Halls for a cancer foundation. Builds relationships with Canadian media, clinicians, researchers, senior leaders, and stakeholders; develops communications strategies, pitches, media materials, crisis plans, executive messaging, and compelling narratives from complex scientific and medical information. Provides strategic counsel, coaches colleagues, manages reputational risks, and coordinates communications between the Foundation and Cancer Centre.

Supports mass marketing campaigns for cancer fundraising events and the Princess Margaret brand. Coordinates briefs, creative development, media launch readiness, vendors, agencies, budgets, campaign documentation, research, reporting, and brand compliance. Collaborates with internal teams and external partners, maintains trackers and approvals, and provides event marketing support, including occasional evening, weekend, and local travel requirements.

Develop and deploy machine learning pipelines and advanced AI models for drug discovery using complex biomedical and DNA-Encoded Library datasets. Responsibilities include data preprocessing, predictive modeling, deep learning, exploratory analysis, visualization, MLOps, experiment tracking, and reproducible workflows. Collaborate with structural biologists, medicinal chemists, and bioinformaticians, communicate findings to diverse audiences, and evaluate emerging approaches for molecular property prediction and de novo drug design.

Leads new product introductions, design transfers, manufacturing readiness, equipment qualification, process validation, and production launch. Develops and optimizes processes, tooling, fixtures, documentation, and assembly methods while improving quality, yield, capacity, and cost. Conducts root-cause investigations, CAPA activities, engineering changes, and manufacturing risk assessments. Provides technical support and mentorship to engineers and technicians while coordinating cross-functional projects with R&D, Quality, Regulatory Affairs, and Operations.

Negotiates, drafts, reviews, and manages clinical trial and research agreements, including confidentiality, collaboration, material transfer, and data sharing agreements. Assesses study complexity, ensures compliance with institutional policies and privacy regulations, manages risk, resolves contractual issues, and coordinates with researchers, ethics boards, financial services, and management. The role also maintains contract documentation and contributes to SOP and review-tool development.