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
Key Responsibilities
- Lead pharmacovigilance activities and risk mitigation strategies for assigned oncology assets and clinical trials
- Drive the evaluation and interpretation of safety data, including signal detection and assessment
- Develop strategic approaches for safety issue evaluation within clinical development programmes
- Contribute to safety components of global regulatory submissions (e.g., INDs, DSURs, IBs)
- Perform literature review, clinical data synthesis, and integrated safety analyses to inform decision-making
- Ensure high-quality, timely delivery while managing multiple priorities
- Represent Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project Teams
- Lead cross-functional efforts to address urgent and complex product safety issues
- Partner closely with Safety Physicians and stakeholders to prepare for and contribute to Safety Review Team (SRT) meetings
- Escalate emerging safety issues to senior leadership and governance bodies as appropriate
- Build strong working relationships and lead effectively within a global matrix organisation
- Coach and mentor colleagues as appropriate
- Present safety recommendations and emerging risks to senior governance committees
- Represent GSK in interactions with regulatory authorities, external experts, and partners
- Apply strategic thinking to evaluate internal and external factors influencing safety decisions
- Contribute to the development of long-term safety and clinical programme strategies
- Identify opportunities for continuous improvement and innovation in safety evaluation processes
- Communicate complex scientific information clearly to a range of audiences
Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Degree in a health-related discipline (e.g., Life Sciences, Pharmacy, Medicine, Nursing), with significant relevant experience
- Substantial experience in pharmacovigilance, drug safety, or a related function within the pharmaceutical or biotechnology industry
- Experience supporting safety in oncology clinical development programmes
- Strong expertise in:
- Signal detection and risk assessment
- Clinical trial safety oversight
- Regulatory safety documentation and submissions
- Knowledge of global pharmacovigilance regulations (e.g., ICH, GVP, CIOMS)
- Proven ability to work effectively in a complex, global matrix environment
- Strong analytical, communication, and problem-solving skills
Preferred Qualification
If you have the following characteristics, it would be a plus:
- Advanced degree (e.g., PhD, PharmD, MD or equivalent)
- Experience interacting with global regulatory authorities
- Experience presenting to senior governance or safety review committees
- Demonstrated leadership experience, including mentoring or team leadership in a matrix setting
- Track record of influencing cross-functional teams and contributing to strategic decision-making
- Experience supporting late-stage clinical development programmes
Working arrangement
This is a hybrid role based in the United Kingdom with a mix of office and remote working. Some travel may be required for meetings and regulatory interactions.
What we value
We seek people who work with integrity, focus on patients and collaborate respectfully. We welcome different perspectives and promote inclusion in our teams. We support development and learning so you can grow while making a meaningful impact on patient safety.
Apply now
If you are ready to use your scientific expertise to protect patients and shape global safety strategy, we would like to hear from you. Please submit your CV and a short cover letter explaining what motivates you to take on this role.
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 we’re 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 [email protected] 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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GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
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Skills Required
- Degree in a health-related discipline (Life Sciences, Pharmacy, Medicine, Nursing)
- Substantial experience in pharmacovigilance, drug safety, or related function within pharmaceutical or biotech industry
- Experience supporting safety in oncology clinical development programmes
- Expertise in signal detection and risk assessment
- Experience in clinical trial safety oversight
- Experience preparing regulatory safety documentation and submissions (e.g., INDs, DSURs, IBs)
- Knowledge of global pharmacovigilance regulations (e.g., ICH, GVP, CIOMS)
- Proven ability to work effectively in a complex, global matrix environment
- Strong analytical, communication, and problem-solving skills
- Advanced degree (PhD, PharmD, MD or equivalent)
- Experience interacting with global regulatory authorities
- Experience presenting to senior governance or safety review committees
- Demonstrated leadership experience, including mentoring or team leadership in a matrix setting
- Experience supporting late-stage clinical development programmes
GSK Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about GSK and has not been reviewed or approved by GSK.
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Strong & Reliable Incentives — Compensation is characterized as including strong salary and perks, with annual bonuses and long-term incentives contributing materially to total rewards. Recognition and performance-linked rewards are described as a consistent component of the package.
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Healthcare Strength — Health coverage is presented as comprehensive, spanning medical, dental, vision, disability, life insurance, and mental health benefits. The breadth of coverage is repeatedly framed as a standout element of the overall rewards experience.
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Retirement Support — Retirement offerings are described as robust, anchored by a 401(k) plan and additional savings vehicles such as employee stock purchase programs. Employer contributions and savings options are portrayed as meaningful supports for long-term financial security.
GSK Insights
What We Do
A science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have three global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products. We aim to bring differentiated, high-quality and needed healthcare products to as many people as possible, with our three global businesses, scientific and technical know-how and talented people.
