# SERM Associate Scientific Director at GSK

GSK is hiring an SERM Associate Scientific Director in London, United Kingdom. Level rates it Little AI ●○○○; you can [apply on GSK](https://jobsbylevel.com/go/cf0efe55-313c-4428-a65a-a8a12ad55c53?utm_medium=ai-agent).

AI Level 1, AI centrality 36 out of 100. Remote (UK – London – New Oxford Street).

## Details

- Company: [GSK](https://jobsbylevel.com/companies/gsk)
- AI level: AI Level 1 (score 36 out of 100)
- Location: Remote (UK – London – New Oxford Street)
- Posted: November 10, 2026
- Apply: https://jobsbylevel.com/go/cf0efe55-313c-4428-a65a-a8a12ad55c53?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=serm-associate-scientific-director-at-gsk-21e39a

## Description

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 international pharmacovigilance guidelines and drug development and approval processes - Experience working effectively in cross-functional, matrix teams - Strong scientific writing skills with the ability to prepare detailed safety evaluations and regulatory documents - Ability to manage multiple tasks with attention to detail and deliver high-quality results on time Preferred Qualification If you have the following characteristics, it would be a plus: - Advanced degree (e.g., PhD, MD, or equivalent) - Previous experience working in large, global pharmaceutical organizations - Familiarity with early clinical development safety activities - Experience contributing to safety governance and regulatory inspections or audits - Knowledge of relevant safety databases and data visualisation tools - Comfortable working in a hybrid model that combines remote and on-site work Work Model This position offers a hybrid working model, supporting flexible working between home and our UK offices. We encourage you to apply and share how your skills and experience will help us ensure patient safety globally. Join us in a role where your expertise will make a meaningful difference every day. Find your career with purpose at GSK. Skills Digital Fluency, Enterprise Leadership, Influencing Without Authority,

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/serm-associate-scientific-director-at-gsk-21e39a

Source: https://jobsbylevel.com/jobs/serm-associate-scientific-director-at-gsk-21e39a

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