NIS P&D Study Delivery Lead, Associate Director Site Name: UK - Hertfordshire - Stevenage, Belgium-Wavre, GSK HQ, USA - Pennsylvania - Upper Providence Posted Date: Dec 18 2025 Closing Date for Applications: 4th January 2026. Key Responsibilities

Plan and lead the delivery of assigned studies to timelines, quality, budget, company standards and scientific requirements; from concept to final study report and archiving. Include the assessment, selection, engagement, and management of appropriate vendors. Act as the primary contact for vendor at study level. Ensure compliance with ICH/GCP & ENCePP guidelines and/or applicable guidelines for NIS such as Good Pharmacovigilance Practices (GVP), Good Epidemiological Practices (GEP) and CIOMS, all applicable laws and regulations, and GSK SOPs, for all products and services delivered for their designated studies. Proactively generate ideas for above-study improvements and implement new business processes and strategies, driving innovative approaches to study delivery through external facing advances in technology and sciences. Support the technical and leadership development of NIS Planning & Delivery staff through mentoring and coaching. May also be responsible for line managing NIS P&D Study Delivery Leads and/or industrial placement students.

Basic Qualifications & Skills

Bachelor's degree in life sciences or related discipline. Proven experience in clinical operations or related research. In-depth knowledge of end-to-end study management, essential regulatory guidelines worldwide, and the clinical development process. Excellent leadership, influencing and negotiation skills. Ability to work independently and proactively and to take on leadership roles on cross-functional teams. Ability to build strong relationships and collaborate successfully, managing trusted stakeholder relationships internally and externally at all levels in a highly dynamic and matrixed environment. Experience managing vendors.

Preferred Qualifications & Skills

Advanced degree (e.g. MS, PhD, PharmD) or equivalent experience. Knowledge and experience of Non-Interventional Studies (NIS). Proven expertise in the proactive identification of issues which may impact clinical programmes coupled with the ability to contribute to solutions affecting cross‑functional matrix teams. Demonstrated experience leading in both matrix and line environments to deliver projects, develop clinical plans, and manage change. Proven experience in managing relationships with vendors to ensure successful delivery of projects.

Benefits

Competitive salary and an annual bonus based on company performance. Healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. Hybrid working model under the Performance with Choice programme, allowing a balance between remote and in‑office work.

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. #J-18808-Ljbffr