Remote Associate Director, Site Engagement & Partnerships

GSK plc; United States; Remote; USD 147,000 - 199,000; Full time

Benefits offered by this job

Health care and other insurance

Retirement benefits

Paid holidays

Vacation

Paid caregiver/parental leave

Job summary

GSK plc seeks an Associate Director Site Engagement to build and oversee a nationwide network of key Oncology sites, balancing regulatory and operational needs. You will shape partnerships, drive study performance, and advocate for digital solutions across LOC and Medical Affairs. Strong leadership and GCP expertise required.

The role emphasizes strategic surveillance, site model development, and proactive risk mitigation to accelerate high-quality trial outcomes in the US.

Qualifications

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

Responsibilities

• Conduct strategic environmental surveillance to anticipate regulatory and operational changes affecting sites and R&D in the United States.
• Lead development and expansion of a US site network spanning academic centers, community practices, and emerging site models.
• Drive performance with KPI targets and regular reviews with external partners; address site-specific challenges.
• Collaborate with Feasibility, Clinical Operations, and Medical Affairs to drive optimal site placement and study performance.
• Drive adoption of enterprise and digital solutions (eConsent, eReg, remote SIVs, EMR monitoring).
• Provide strategic input for operational excellence and share best practices across LOC/region/global site network.

Skills

Agile Thinking

Business Acumen

Clinical Development

Clinical Trial Designs

Communication

Creativity

Decision Making

Fostering Collaboration

Good Clinical Practice

Influencing Without Authority

People Management

Pharmaceutical Industry

Project Management

Time Management

Education

Bachelor's degree

Job description

GSK plc seeks an Associate Director Site Engagement to build and oversee a nationwide network of key Oncology sites, balancing regulatory and operational needs. You will shape partnerships, drive study performance, and advocate for digital solutions across LOC and Medical Affairs. Strong leadership and GCP expertise required.

The role emphasizes strategic surveillance, site model development, and proactive risk mitigation to accelerate high-quality trial outcomes in the US.