Site Engagement Associate Director - Hepatology
GSK
September 03, 2026
Remote friendly (Philadelphia, PA)
United States
Clinical Research and Development
Associate Director Site Engagement – Oncology
Responsibilities:
- Conduct strategic environmental surveillance to anticipate regulatory/operational changes affecting US sites and R&D; design innovative partnerships.
- Build and expand a US site partnership network (academic centers, community practices, hybrid/DCT-enabled sites); act as main point of contact.
- Lead development and expansion of the US site network; provide updates and feedback to Leadership/Local Medical Affairs (LOC).
- Drive performance via mutually agreed KPI targets; conduct periodic performance reviews; track action plans; implement solutions to reduce cycle times and optimize enrollment; participate in/lead site visits.
- Identify and mitigate bottlenecks and risks to quality/compliance; develop and implement mitigation/corrective actions with sites and LOC Clinical Operations.
- Collaborate with Feasibility, Clinical Operations, and Medical Affairs to drive optimal site placement and study performance.
- Drive adoption of digital/centralized solutions (eConsent, eReg, remote SIVs, EMR-based ID, remote EMR monitoring access).
- Provide strategic operational input on future therapeutic areas/portfolio to external stakeholders.
- Share best practices to improve process efficiency and trial delivery; develop unique site models.
Basic Qualifications:
- Bachelor’s degree in life science (or equivalent experience).
- 5+ years’ clinical research operations experience.
Preferred Experience:
- Travel up to 60% (domestic).
- Experience in respiratory and/or hepatology.
- Knowledge of drug development process; clinical study process/monitoring.
- Track record establishing/growing strategic site/institution partnerships.
Skills:
Agile thinking, business acumen, clinical development/trial design, communication, influencing without authority, collaboration, GCP, people/project/time management.
Benefits:
- Annual bonus; eligibility for share-based long-term incentive; health/insurance, retirement, paid holidays/vacation, and paid caregiver/parental & medical leave.
Application instructions:
- For accommodations, contact usrecruitment.adjustments@gsk.com.
Responsibilities:
- Conduct strategic environmental surveillance to anticipate regulatory/operational changes affecting US sites and R&D; design innovative partnerships.
- Build and expand a US site partnership network (academic centers, community practices, hybrid/DCT-enabled sites); act as main point of contact.
- Lead development and expansion of the US site network; provide updates and feedback to Leadership/Local Medical Affairs (LOC).
- Drive performance via mutually agreed KPI targets; conduct periodic performance reviews; track action plans; implement solutions to reduce cycle times and optimize enrollment; participate in/lead site visits.
- Identify and mitigate bottlenecks and risks to quality/compliance; develop and implement mitigation/corrective actions with sites and LOC Clinical Operations.
- Collaborate with Feasibility, Clinical Operations, and Medical Affairs to drive optimal site placement and study performance.
- Drive adoption of digital/centralized solutions (eConsent, eReg, remote SIVs, EMR-based ID, remote EMR monitoring access).
- Provide strategic operational input on future therapeutic areas/portfolio to external stakeholders.
- Share best practices to improve process efficiency and trial delivery; develop unique site models.
Basic Qualifications:
- Bachelor’s degree in life science (or equivalent experience).
- 5+ years’ clinical research operations experience.
Preferred Experience:
- Travel up to 60% (domestic).
- Experience in respiratory and/or hepatology.
- Knowledge of drug development process; clinical study process/monitoring.
- Track record establishing/growing strategic site/institution partnerships.
Skills:
Agile thinking, business acumen, clinical development/trial design, communication, influencing without authority, collaboration, GCP, people/project/time management.
Benefits:
- Annual bonus; eligibility for share-based long-term incentive; health/insurance, retirement, paid holidays/vacation, and paid caregiver/parental & medical leave.
Application instructions:
- For accommodations, contact usrecruitment.adjustments@gsk.com.