Location: UK - Hertfordshire - Stevenage, Belgium-Wavre
NIS P&D Study Delivery Lead, Associate Director
Primary responsibility is to lead the full lifecycle of clinical studies and trials within the Non Interventional Study (NIS) portfolio, including designing, executing, and reporting studies, complex regulatory commitment studies, and large multi‑centre, multi‑country primary data studies. The role may also involve leading and managing team members within the NIS P&D Team.
Responsibilities
* Plan and lead delivery of assigned studies to meet timelines, quality, budget, and scientific requirements from concept to final report and archiving.
* Coordinate and deliver study protocols, informed consent forms, and clinical study reports.
* Develop and execute study delivery strategy including country selection, diversity, patient engagement, and recruitment plans.
* Manage vendor selection, engagement, and performance.
* Manage study‑level budgets in alignment with project allocations.
* Lead operational decision‑making, risk management, and issue escalation.
* Build strong cross‑functional partnerships across global teams.
* Ensure compliance with ICH/GCP, ENCePP, GVP, GEP, and applicable regulations and SOPs.
* Drive innovation in study delivery through new technologies and approaches.
* Support development and mentoring of team members.
Basic Qualifications & Skills
* Strong leadership, influencing, and negotiation skills.
* Experience managing performance and developing talent.
* Excellent decision‑making and problem‑solving ability.
* Ability to work independently and lead cross‑functional teams.
* Budgeting, forecasting, and financial acumen.
* Bachelor’s degree in life sciences or related discipline.
* Experience in clinical operations or research.
* Knowledge of regulatory guidelines and clinical development processes.
Preferred Qualifications & Skills
* Advanced degree (MS, PhD, PharmD) or equivalent experience.
* Experience in non‑interventional studies (NIS).
* Ability to identify and resolve issues impacting clinical programmes.
* Experience leading in matrix and line environments.
* Vendor management experience.
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.
Application close date: COB 01/06/26.
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