SERM Associate Scientific Director

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 people’s 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. We’re uniting science, technology, and talent to get ahead of disease together.

Find out more:

Our approach to R&D

Position Summary

Join GSK as a SERM Associate Scientific Director in the United Kingdom and use your medical and scientific expertise to support patient safety worldwide. You will work closely with cross-functional teams to evaluate safety data and manage risks across key products in clinical development and the post-marketing setting. Your clear, thoughtful insights will help shape decision-making and improve outcomes for patients and healthcare professionals. We value collaboration, integrity, and a growth mindset, providing a place where you can thrive and make an impact through science, technology, and talent united to get ahead of disease together.

Responsibilities

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Lead or contribute signal detection and evaluation activities for assigned products, applying strong scientific judgment.
• Prepare and review global regulatory reports and risk management plans, ensuring accuracy and timely delivery.
• Support safety governance meetings and collaborative safety review teams for clinical and post-marketing safety oversight.
• Contribute to the design and implementation of risk-reduction strategies in clinical protocols and product information.
• Build and maintain effective relationships across teams, providing clear communication and mentoring colleagues where appropriate.
• Participate in process improvements to enhance compliance, quality, and efficiency within safety evaluation activities.

Why You?

Basic Qualification

We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• A degree in Health Sciences or Healthcare Professional qualification (for example, BSc, MSc, PhD, RN, NP, PharmD)
• Practical experience in pharmacovigilance focusing on safety evaluation and risk management during clinical development and post-marketing phases
• Understanding of interna...

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat. Duis aute irure dolor in reprehenderit in voluptate velit esse cillum dolore eu fugiat nulla pariatur. Excepteur sint occaecat cupidatat non proident, sunt in culpa qui officia deserunt mollit anim id est laborum.

Sed ut perspiciatis unde omnis iste natus error sit voluptatem accusantium doloremque laudantium, totam rem aperiam, eaque ipsa quae ab illo inventore veritatis.