Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Canada - Ontario - Mississauga, GSK HQ, UK - Hertfordshire - Stevenage, USA - Massachusetts - Waltham, Warsaw
Posted Date: Mar 31 2026
Job Purpose
The primary responsibility of the NIS P&D TA Study Delivery Head is to lead a team of Study Delivery Leads (SDLs) in executing Non-Interventional Studies (NIS) within their designated therapy area (TA). These studies align with integrated evidence plans across both the Research & Development (R&D) and marketed product portfolios. The role collaborates with functional leaders such as the Global Real-World Evidence & Health Outcomes (gRWE&HO) TA Head, the Epidemiology TA Head, and the NIS P&D TA Project Management Head to ensure successful delivery of study outcomes in terms of timelines, quality, and budget. The position is part of the NIS P&D Leadership Team.
Key Responsibilities
* Lead and develop a team of Study Delivery Leads, accountable for optimal study delivery support models.
* Partner with TA and functional stakeholders to optimize NIS study timelines and scenarios, enabling delivery of Global Epidemiology, Data Generation, and Clinical Development Plans.
* Collaborate with TA-aligned functions, building strong relationships and influencing across Global Clinical Operations.
* Contribute to asset and study governance and protocol development to ensure operational feasibility, consistency, quality, cost efficiency, and timely delivery.
* Plan, prioritize, and allocate TA resources in line with business priorities; oversee hiring, performance management, coaching, and development.
* Ensure compliance with ICH/GCP, ENCePP, GVP, GEP, CIOMS, applicable regulations, and GSK SOPs.
* Drive innovation in study delivery through advances in technology and science.
* Support early feasibility and engagement activities prior to SDL assignment.
* Lead or contribute to global, cross‑functional business improvement initiatives across R&D and CPO.
* Implement new business processes and strategies.
* Manage and oversee FSO/FSP vendor relationships, acting as escalation point and driving continuous improvement.
Basic Qualifications
* Bachelor’s degree in life sciences or related discipline.
* Ten years minimum experience in clinical operations or related research.
* Five or more years of expertise and experience in Non-Interventional Studies (NIS) with a strong background in the Oncology Therapy Area.
* Five or more years of experience leading a team.
Preferred Qualifications
* Advanced degree (e.g., MS, PhD, PharmD) or equivalent experience.
* Proven experience in managing vendor relationships to ensure effective resourcing strategies and successful project delivery.
* Proven ability to define the best decision for the organization, not one function.
* Proven expertise in proactively identifying issues that may impact clinical programmes and contributing solutions for cross‑functional matrix teams.
* Demonstrated experience leading both matrix and line environments to deliver projects, develop clinical plans, and manage change.
Benefits
* Annual bonus and participation in a share‑based long‑term incentive program (role dependent).
* Health‑care and other insurance benefits for employee and family.
* Retirement benefits.
* Paid holidays, vacation, and paid caregiver/parental and medical leave.
Salary information for the United States will be discussed during the recruitment process. For additional compensation details, candidates will receive more information upon request.
Equal Opportunity Employer
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service, or any basis prohibited under federal, state or local law.
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