NIS P&D Oncology Study Delivery Head

Overview

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Canada - Ontario - Mississauga, GSK HQ, UK - Hertfordshire - Stevenage, USA - Massachusetts - Waltham, Warsaw

Posted Date:
Jan 30 2026

GSK's success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued and included.

Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

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 are aligned with the integrated evidence plans across both the Research & Development (R&D) and marketed product portfolios. The role involves close collaboration with functional leaders in the NIS portfolio, 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 the successful delivery of study outcomes (including timelines, quality, and budget).

The NIS P&D TA Study Delivery Head is accountable for the operational execution of the TA portfolio, working within the established operational support model. This 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.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• 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:

If you have the following characteristics, it would be a plus:

• Advanced degree (e.g. MS, PhD, Pharm
  
  D) 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 and not one function.
• 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 environment to deliver projects, develop clinical plans, and manage change

#LI-GSK*

Salary and benefits

* If you are based in Cambridge, MA;
Waltham, MA;
Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $189,750 to $316,250.

The US salary ranges take into account a number of factors including work location within the US market, the candidate's skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process. The annual base salary in Poland for new hires in this position ranges from PLN 429,000 to PLN 715,000 gross, taking…