Site Engagement Associate Director- Oncology

Position Summary

Through leadership, the Site Engagement Associate Director-Oncology is accountable for developing, managing, and overseeing long-term and strong relationships with strategically and operationally important Oncology sites and institutions. It includes building and enhancing the image and reputation of GSK with sites locally and providing an interface between GSK and the sites to create an optimal clinical trials environment to generate results in a timely manner with high quality outputs.

**NOTE: for serious consideration, candidates must currently reside within the following geographic areas in the continental US:

• West Coast: California, Oregon, Nevada, Washington State

• South /Central: Texas, Colorado, Louisiana, Arkansas

Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Conduct strategic environmental surveillance in oncology to anticipate regulatory and operational changes affecting sites and R&D in the United States, and use those insights to design innovative, efficient partnerships.

• Provide insight to leadership on site landscape trends, operational risks, and emerging engagement models.

• Lead the development and expansion of a US oncology site network spanning academic centers, community practices, and emerging site model (hybrid networks, DCT enabled sites.

• Enhance collaboration between sites and GSK clinical teams to improve performance and resolve obstacles during site start‑up and study execution.

• Create and implement strategic partnership models and frameworks for strategic clinical sites.

• Build and nurture relationships with community sites, engaging local investigators and staff to expand the GSK partnership network

• Give an operational vision of the future GSK portfolio (collaborating with LOC MED) to key external stakeholders in order to anticipate partnerships and to help them to better prepare the arrival of clinical trials

• Provide strategic input for operational excellence, process efficiency and trial delivery both internally and externally

• Identify and disseminate best practices and contribute to standardization across local operations

• Track compliance with site partnership agreements, pinpoint problem areas, and take corrective actions to ensure successful outcomes.

• Collaborate, communicate, and resolve key operational issues with external site partners.

• Drive performance, by putting in place mutually agreed KPIs (quality and performance) and organizing periodic review with the different external partners

• Provide feedback to Leadership, Local Medical Affairs, LOC regarding the development of new partnerships and updates on existing ones.

• Responsible for standardizing processes, identifying and sharing best practices at internal cross functional process improvement teams.

• Champion patient centric solutions and representative strategies tailored to U.S. oncology populations.

• Collaborate with Feasibility, Clinical Operations, and Medical Affairs to drive optimal site placement and study performance.

• Partner with cross functional teams to optimize site activation timelines (regulatory packets, budgets/CTAs, onboarding, training).

• Identify bottlenecks at both the study and site level and implement targeted solutions to reduce cycle times.

• Drive adoption of digital and centralized solutions (e.g., eReg, remote SIVs, EMR- based identification).

• Build and maintain strong, trusted relationships with investigators, research coordinators, and site leadership.

• Participate in site visits to deliver targeted operational support and address site-specific challenges.

• Serve as an escalation point for site performance issues and proactively implement site specific action plans.

• Consider and develop unique site models, further enhancing portfolio of sites to include in studies.

Why You?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• Bachelor's degree in related discipline, preferably in life science.

• 5 + years' experience in clinical research operations.

• 3 + years' experience in Oncology clinical research.

Preferred Qualification
If you have the following characteristics, it would be a plus:

• Good knowledge of the Drug Development Process.

• Excellent understanding of the Clinical