Clinical Research Engagement Lead (CREL) Job Roche

Are you passionate about strengthening healthcare partnerships to accelerate clinical innovation? As the Clinical Research Engagement Lead (CREL), you will play a pivotal role in driving strategic site engagement, optimizing clinical trial operations, and delivering an exceptional, streamlined experience for clinical trial sites.
In this role, you will champion a “One Roche” approach, acting as the primary point of contact for strategic sites and bringing together internal medical and operational teams to anticipate and support site needs. By establishing a collaborative local community and managing key relationships with Contract Research Organizations (CROs), you will ensure the successful, high-quality delivery of our portfolio from early to late-stage clinical development.

Key Responsibilities:

• Drive Strategic Site Engagement: Develop and execute tailored country-level site engagement strategies across disease areas, fostering trust, operational excellence, and accelerated trial progression.
• Optimize Early Landscaping & Feasibility: Engage strategically with investigators during early trial setup, landscaping, and protocol review phases to identify the most suitable sites and optimize recruitment speed.
• Lead Relationship Management & Collaboration: Act as the primary point of contact for strategic clinical sites, building deep connections with investigators, pharmacists, and clinic administrations to align cross-study priorities and capture feedback trends.
• Coordinate Internal Communities: Convene and lead a local site engagement community (integrating Local Medical Affairs, field medical teams, and clinical operations) to streamline communications and enhance the site experience.
• Provide Global & Local Study Oversight: Oversee the planning, risk mitigation, and compliance of assigned clinical studies, tracking monitoring performance, risk-based monitoring plans, and trial master file completeness.
• Manage Partner Relationships: Collaborate closely with CRO partners throughout the clinical trial lifecycle to ensure unified delivery goals, high site satisfaction, and swift resolution of operational challenges.
• Ensure Inspection Readiness: Lead local quality reviews, internal audits, and regulatory inspections for allocated studies, ensuring absolute compliance with global quality standards and regulatory guidelines.

Who You Are

• You are a strategic, relationship-driven clinical operations professional who excels in dynamic environments, leads cross-functional alignment through ambiguity, and holds a strong commitment to customer-centric delivery.

Qualifications & Skills:

• Education: Degree (MD, PhD, Master’s, or Bachelor’s) in life sciences or an equivalent discipline.
• Experience: Significant experience in the pharmaceutical or clinical research industry, with essential expertise in end-to-end product development and clinical trial processes.
• Relationship Management: A proven track record of managing site relationships, overseeing complex clinical trials, and effectively collaborating with CROs.
• Strategic & Analytical Mindset: Demonstrated ability to handle multiple priorities, proactively identify operational challenges, and develop effective, data-backed compliance and mitigation strategies.
• Communication & Influencing: Exceptional presentation, interpersonal, and negotiation skills, with the ability to bridge communication gaps between global teams and local external stakeholders.
• Languages: Mandatory fluency in written and spoken English, as well as the local language(s) of the host country.
• Mobility: Willingness and flexibility to travel to trial sites on an ongoing basis to establish and maintain strong relationships (frequent domestic and occasional international travel required).

How to Apply

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