[Hiring] Site Engagement Associate Director @GSK

Role Description

Through leadership, the Associate Director Site Engagement 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.

• Conduct strategic environmental surveillance to anticipate regulatory and operational changes affecting sites and R&D in the United States, and use those insights to design innovative, efficient partnerships.
• Contribute to the development of a strategic partnership network, acting as the main point of contact between GSK and sites.
• Lead the development and expansion of a US site network spanning academic centers, community practices, and emerging site model (hybrid networks, DCT enabled sites).
• Provide feedback to Leadership, Local Medical Affairs, LOC regarding the development of new partnerships and updates on existing ones.
• Drive performance by putting in place mutually agreed KPI targets (quality and performance) and organizing regular, periodic performance reviews with the different external partners.
• Work closely with sites and with all members of the LOC Clinical Operations Department to proactively identify bottlenecks at both the study and site level and any risks to quality and compliance.
• Collaborate with Feasibility, Clinical Operations, and Medical Affairs to drive optimal site placement and study performance.
• Drive adoption of enterprise and other digital and centralized solutions (e.g., eConsent, eReg, remote SIVs, EMR-based identification and remote EMR monitoring access).
• Conduct ongoing environmental strategic surveillance and anticipate the legislative and practical evolution of sites and R&D in the country.
• Provide strategic input for operational excellence, process efficiency, and trial delivery both internally and externally.
• Consider and develop unique site models, further enhancing the portfolio of sites to include in studies.

Qualifications

• Bachelor's degree required, or 5+ years of relevant Clinical Operations experience.

Requirements

• Ability to travel up to 60% (Domestic).
• Experience in respiratory and/or hepatology.
• Proficient knowledge of the Drug Development Process.
• Excellent understanding of the Clinical Study Process, including monitoring.
• Demonstrated track record of establishing and growing partnerships with strategic sites/institutions.

Benefits

• US annual base salary ranges from $129,750 to $216,250.
• Annual bonus and eligibility to participate in share-based long-term incentive program.
• Health care and other insurance benefits (for employee and family).
• Retirement benefits.
• Paid holidays and vacation.
• Paid caregiver/parental and medical leave.