Evidence Operations Manager

About Roche

The Position

Operational Ownership and Study Management

• Lead assigned evidence-generation studies and programs, owning operational milestones, budget, scope, and strategic alignment.
• Manage daily study operations, including investigational medicinal product management, budget oversight, milestone tracking, and accurate trial database maintenance.

Vendors, Compliance, and Feasibility

• Partner with sponsors, research sites, and vendors to ensure quality deliverables comply with budgets, ICH-GCP standards, local regulations, and Roche SOPs.
• Provide operational expertise during conceptualization, feasibility, start-up, and conduct phases and proactively identify and mitigate risks.

Process Excellence and Collaboration

• Evaluate workflows, identify efficiencies, solve complex operational challenges, and contribute to clinical operations excellence.
• Act as the primary operational contact for assigned studies and build collaborative relationships with internal and external stakeholders.

Required Qualifications

• A bachelor’s degree in a medical or science-related discipline is required.
• Two to four years of experience in clinical research or the broader health industry is required.
• Knowledge of clinical trial management operations, ICH-GCP standards, and relevant regulatory frameworks is required.
• Strong project management, organizational, communication, presentation, and problem-solving abilities are required.

Preferred Qualifications

• A master’s degree in science or a postgraduate diploma in clinical research is preferred.
• French language skills, digital literacy, office and collaboration platforms, clinical data management systems, therapeutic-area familiarity, and strategic project oversight are preferred.

Compensation

• The expected hiring range for the primary Mississauga location is 105,560.00 to 138,547.50, with actual pay based on experience, qualifications, and other job-related factors.