Executive Medical Director, SERM Scientific Excellence

Business Introduction
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 lives. GSK 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.
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Our approach to R&D


Position Summary

The Executive Medical Director Safety Evaluation and Risk Management (SERM) Scientific Excellence is an integral figure within GSKs Global Safety team reporting to the Vice President and Head of Vaccines and Infectious Disease Safety. This senior-level role focuses on advancing scientific safety standards and practices predominantly within Vaccines SERM but also across other therapeutic areas when needed. You will play role in shaping safety approaches for early-phase and non-pivotal trials as well as studies involving vulnerable populations.

As the study-independent chair of the internal Safety Review Committee (iSRC) you will also ensures the scientifically sound review and interpretation of unblinded safety data protecting trial participants while maintaining the integrity of clinical trials. .

This multifaceted position provides an opportunity to be a pivotal driver in enhancing patient safety during early clinical development phases setting global standards for safety governance and cultivating a high-performing culture within GSK. Successful candidates will bring deep expertise in clinical practice drug safety / pharmacovigilance and scientific data analysis combined with leadership capabilities to build cross-functional relationships and drive forward GSKs mission of delivering innovative healthcare solutions to patients worldwide.

Key Responsibilities:

• Lead the definition maintenance and implementation of standardised and compliant safety approaches for first-in-human early-phase trials and studies involving vulnerable populations while adapting strategies to align with evolving regulatory expectations.
• Serve as the study-independent chair of the internal Safety Review Committee (iSRC) driving scientifically robust reviews and guiding the interpretation of unblinded safety data to ensure participant protection and safeguard trial integrity.
• Collaborate with study teams to establish appropriate safety endpoints monitoring and surveillance methods risk mitigation strategies and plans for the timely analysis of emerging safety signals.
• Guide decision-making processes in critical review bodies such as Data Monitoring Committees and Dose Escalation Committees to ensure the proper escalation and response to safety concerns.
• Oversee the readiness and optimisation of systems for safety data collection reporting and analysis throughout clinical trial preparation and execution enabling proactive signal detection and mitigation.
• Provide leadership in developing scientific capabilities within SERM teams by coaching physicians and scientists introducing innovative analytical approaches and fostering continuous learning and improvement.
• Serve as a culture champion for high performance within Global Safety while actively contributing to strategies for the evaluation and management of urgent product safety issues.

Why You

Basic Qualifications:

• Medical Doctor
• Completion of a primary postgraduate clinical training clinical residency or specialty training.
• Extensive hands-on safety and pharmacovigilance knowledge and expertise in scientific safety data analysis interpretation and evaluation.
• Proficiency in applying frameworks for reviewing unblinded safety data with meticulous attention to study integrity.
• Solid understanding in vaccinology epidemiology and biostatistics as applied to clinical safety analysis.

Preferred Qualification

• Proven track record of identifying and addressing capability gaps within teams through the design and execution of formal development programs.
• Exceptional communication skills enabling clear and impactful presentation of complex scientific data to internal and external audiences alike.
• Leadership experience in developing talent fostering collaboration driving change management and cultivating a high-performing operational culture especially in cross-functional global environments.
• Creative problem-solving expertise and sound judgment in critical safety situations while maintaining a strategic and tactical view of organisational goals.

Location and Working Arrangements
- This role can be based in the United Kingdom Belgium or Italy.
- Hybrid working is supported with regular on-site collaboration expected to build effective teamwork and stakeholder relationships.

What we offer
You will join a global organisation focused on meaningful patient impact. You will have opportunities to grow your career lead high-value projects and work with committed colleagues who share a clear purpose. We encourage an inclusive culture where different perspectives are welcomed and where your work will contribute to getting ahead of disease together.

Ready to make an impact We would love to hear from you. Apply now to join our team and help shape the future of patient care.

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.

We believe in an agile working culture for all our roles. If flexibility is important to you we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call.

Please note should your enquiry not relate to adjustments we will not be able to support you through these channels. However we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

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