NIS P&D Study Delivery Lead, Associate Director

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NIS P&D Study Delivery Lead Associate Director

The primary responsibility of the Non-Interventional Study (NIS) Planning and Delivery (P&D) Study Delivery Lead (SDL) Associate Director is to lead the full lifecycle of clinical studies and trials within the NIS portfolio. This includes designing executing and reporting interventional studies complex regulatory commitment studies (such as PASS and registries) and large multicentre multi-country primary data studies.

Additionally this role may involve leading and managing team members within the NIS P&D Team.

The position requires a performance-driven seasoned study management professional with a strong sense of urgency exceptional organisational credibility and deep understanding of the NIS scientific and operational aspects of the pharmaceutical R&D business.

Key Responsibilities include the following:

• Planning and leading the delivery of assigned studies to timelines quality budget company standards and scientific requirements; from concept to final study report and archiving. Including the assessment selection engagement and management of appropriate vendors. Act as the primary contact for vendor at study level.
• Ensures 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 generating ideas for above-study improvements and implementing new business processes and strategies. Driving innovative approaches to study delivery through external facing advances in technology and sciences.
• Supporting the technical and leadership development of NIS Planning & Delivery staff through mentoring and coaching and may also be responsible for line managing NIS P&D Study Delivery Leads and/or industrial placement students.

Why you

Basic Qualifications & Skills

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

• Bachelors 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:

Please note the following skills are not necessary just preferred if you do not have them please still apply:

• 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 environment to deliver projects develop clinical plans and manage change.
• Proven experience in managing relationships with vendors to ensure successful delivery of projects.

Closing Date for Applications 4th January 2026.

Please take a copy of the Job Description as this will not be available post closure of the advert.

When applying for this role please use the cover letter of the online application or your CV to describe how you meet the competencies for this role as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.

At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples fosters a culture ambitious for patients accountable for impact and committed to doing the right thing making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. Were uniting science technology and talent to get ahead of disease together.

Find out more:

Our approach to R&D.

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Why GSK

Uniting science technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive.

We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

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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