Evidence Operations Manager
Roche
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Position
A healthier future. That’s what drives us.
The Evidence Operations Manager (EOM) provides operational expertise and oversight to the Canadian affiliate's research portfolio to ensure the successful, timely execution of strategic, innovative evidence. The EOM oversees and manages the operational implementation of all supported studies (including Investigator Initiated Studies), Managed and Funded Non-Interventional Studies, Scientific Credibility and RWE studies in accordance with the applicable regulatory requirements and guidelines (e.g. AMG, MPG, ICH / GCP etc.) as well as applicable Roche SOPs. As a key partner with your therapeutic area team, you provide portfolio oversight and strategic insights to maximize the feasibility and impact of these activities.
The Opportunity:
- End-to-End Operational Ownership: Lead assigned evidence-generation studies and programs, taking full accountability for delivering operational milestones on time, within budget, scope, and aligned with strategic objectives.
- Trial Management & Platform Tracking: Manage day-to-day operational elements—including IMP management, budget oversight, and key milestone tracking—ensuring trial management databases and tracking tools are maintained accurately in real time.
- Vendor & Stakeholder Oversight: Partner with external sponsors, research sites, and vendor partners to ensure quality deliverables that comply with agreed budgets, ICH-GCP standards, local regulations, and Roche SOPs while proactively identifying and mitigating risks.
- Strategic Input & Feasibility: Provide operational expertise to Medical Affairs strategy hubs during the conceptualization, feasibility, start-up, and conduct phases of evidence-generation activities.
- Process Excellence & Innovation: Continuously evaluate study workflows to identify efficiencies, solve complex operational challenges, and contribute to overall clinical operations excellence.
- Cross-Functional Collaboration: Serve as the primary operational point of contact for assigned studies, building and maintaining collaborative, high-trust relationships with internal and external stakeholders.
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