**Site Name**: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Bengaluru Luxor North Tower, Canada - Ontario - Mississauga - Milverton Drive, GSK HQ, Italy - Rosia, Poznan Grunwaldzka, Poznan Pastelowa, UK - Hertfordshire - Stevenage
**Posted Date**: Mar 20 2026
**Job Purpose**:
You will lead and develop the program level operational strategy and delivery plan for an asset, ensuring studies run safely and efficiently. You will work with cross-functional partners to keep programs inspection ready and to deliver high-quality data for regulatory interactions. We value clear judgement, practical problem solving, and collaborative leadership. This role offers strong learning and career growth, and the chance to make meaningful impact aligned with GSK’s mission of uniting science, technology and talent to get ahead of disease together. **Key Responsibilities**: - Lead asset-level clinical operations planning to maintain inspection readiness and regulatory deliverables.
- Contribute to the development of the Clinical Development Plan and Integrated Evidence Plan
- Represent Global Clinical Operations functions at the asset level.
- Coordinate cross-functional partners (clinical, biostatistics, clinical supplies, safety, and vendors) to support timely data deliveries.
- Oversee vendor selection, contracting input, and operational oversight for outsourced clinical activities.
- Model scenarios for optimal asset/study delivery linked to value drivers and drives decisions presented to governance boards
- Maintain and drive implementation of asset-level operational risk and mitigation plans.
- Drive innovative approaches to study execution through external facing advances in technology and sciences, by identifying and embracing risks and opportunity




- Provide strategic guidance and leadership to Study Delivery Teams to ensure clinical project goals are met.
- Prepare and respond to data requests and contribute to materials for regulatory submissions. **Basic Qualifications**:
**_
We are seeking professionals with the following required skills to achieve our goals:_**
- Advanced degree in MD, PharmD, PhD or related field, or equivalent clinical experience.
- 8+ years of clinical development experience, with oncology exposure.
- 3+ years of experience leading R&D; interventional studies (Phase I, II, III).
- Experience in managing cross-functional, matrixed teams with defined deliverables and performance outcomes.
- Experience in clinical trial design, safety governance and regulatory submission requirements.
- Experience in managing clinical research projects or equivalent in at least 2 different TA
- Experience in project development, quality requirements and associated processes.
- Experience in clinical development and matrix management.
- Create and implement multi-year, cross‑functional operational plans across multiple streams and indications for single asset or multiple interdependent assets.
- Experience converting scientific, strategic, and stakeholder input into documented action plans, timelines, and execution frameworks for the Asset team.
- Experience in coordinating communication, decision inputs, and deliverables with senior leadership, including SVP and C‑suite stakeholders.




- Experience developing and presenting structured reports, analyses, and recommendations that distill complex scientific and operational data into clear decision-ready formats for senior leadership. **Work Arrangements**:
This role is based in Belgium, UK, US, Italy, Canada, Poland or India and follows a hybrid working model. You will be expected on-site some days each week to collaborate with colleagues and study teams. We support flexible remote work when appropriate. More detailed information on the total reward package applicable to your role will be supplied during the recruitment process. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the market rate for the role. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. **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 i

📌 Clinical Operations Director (Oncology) Asset Lead (Siena)
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