At a Glance
- Tasks: Lead safety evaluations and risk management in clinical development and post-marketing.
- Company: Join GSK, a global biopharma company with a mission to impact 2.5 billion lives.
- Benefits: Hybrid working model, career growth opportunities, and a culture focused on patient impact.
- Other info: Collaborate globally and thrive in a culture of innovation and accountability.
- Why this job: Make a meaningful impact on patient safety while advancing your career in a dynamic environment.
- Qualifications: Bachelor's in health sciences; experience in pharmacovigilance or drug safety preferred.
The predicted salary is between 80000 - 100000 € per year.
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.
The SERM Scientific Director provides medical and scientific leadership in the evaluation and management of product safety across clinical development and post-marketing phases. This role is responsible for assessing benefit-risk profiles, identifying and managing safety concerns, and supporting regulatory and governance activities to ensure patient safety. The position operates within a global, cross-functional environment and may include leadership or mentoring responsibilities within a matrix structure.
Key Responsibilities
- Lead pharmacovigilance and risk management strategy across clinical development and post-marketing products
- Evaluate and interpret safety data to inform benefit-risk assessments and support decision-making
- Identify, assess, and escalate safety signals, ensuring appropriate mitigation strategies are implemented
- Contribute to safety components of regulatory submissions and interactions with regulatory authorities
- Represent safety in cross-functional project teams and governance forums
- Support inspection readiness activities and contribute to continuous process improvement initiatives
- Collaborate effectively with internal and external stakeholders to communicate safety information
- Provide leadership, mentoring, or coaching within a matrix environment, where applicable
Minimum Qualifications (Essential)
- Bachelor's Degree in a health sciences or healthcare-related discipline (e.g., life sciences, pharmacy, nursing, or medicine)
- Demonstrated experience in pharmacovigilance, drug safety, or a closely related field
- Experience in safety evaluation and risk management within clinical development and/or post-marketing settings
- Knowledge of global pharmacovigilance regulations and guidelines (e.g., ICH, GVP)
- Experience working within cross-functional or matrix team environments
- Ability to analyse complex data and communicate findings clearly to diverse stakeholders
Preferred Qualifications (Desirable)
- Advanced degree (e.g., MSc, PhD, PharmD, MD, or equivalent)
- SERM Oncology experience
- Experience leading or influencing cross-functional teams or projects
- Experience contributing to regulatory submissions or interactions with health authorities
- Experience supporting audits or inspections in a regulated environment
- Experience within a global pharmaceutical or biotechnology organisation
This role is based in the United Kingdom. The role operates on a hybrid working model with an agreed mix of office and remote work to support collaboration and governance activities.
If this role matches your experience and ambitions, please apply. Share your CV and a short note describing what you would bring to the role and what you want to learn. We welcome applicants who are motivated to make a meaningful impact on patient safety and who want to grow their career within a global safety team.
SERM Scientific Director, Oncology in London employer: Gsk
GSK is an exceptional employer, offering a dynamic and inclusive work environment where innovation thrives. With a strong commitment to employee growth, GSK provides opportunities for professional development and mentorship within a global safety team, all while focusing on making a meaningful impact on patient health. The hybrid working model in the UK allows for flexibility, ensuring that employees can balance collaboration with personal needs, making it an attractive place for those looking to advance their careers in the biopharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land SERM Scientific Director, Oncology in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at GSK or in similar roles. A friendly chat can open doors and give you insider info that could make all the difference.
✨Tip Number 2
Prepare for interviews by diving deep into GSK's mission and values. Show them you’re not just another candidate; you’re someone who genuinely cares about making an impact on patient safety and aligns with their ambitious goals.
✨Tip Number 3
Practice your STAR technique for answering behavioural questions. Structure your responses around Situation, Task, Action, and Result to clearly demonstrate your experience and how it relates to the role.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, you can tailor your CV and cover letter to highlight exactly what you bring to the table for this role.
We think you need these skills to ace SERM Scientific Director, Oncology in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the SERM Scientific Director role. Highlight your experience in pharmacovigilance and risk management, and don’t forget to showcase any relevant leadership roles you've had. We want to see how your background aligns with our mission!
Craft a Compelling Note:When you write your short note, be genuine! Share what excites you about this role and how you can contribute to patient safety. We love seeing passion and motivation, so let your personality shine through!
Showcase Your Skills:Don’t just list your qualifications; explain how they relate to the key responsibilities of the role. If you’ve worked in cross-functional teams or have experience with regulatory submissions, make sure to highlight those experiences clearly. We’re looking for specific examples!
Apply Through Our Website:Remember to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about GSK and our culture while you’re at it!
How to prepare for a job interview at Gsk
✨Know Your Stuff
Make sure you brush up on your pharmacovigilance and risk management knowledge. Understand the latest regulations and guidelines, especially those related to oncology. Being able to discuss these confidently will show that you're serious about the role.
✨Showcase Your Experience
Prepare specific examples from your past work that highlight your experience in safety evaluation and risk management. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easy for the interviewers to see your impact.
✨Engage with the Team
Since this role involves cross-functional collaboration, be ready to discuss how you've worked effectively in team settings before. Share instances where you led or influenced projects, and emphasise your ability to communicate complex data clearly to diverse stakeholders.
✨Ask Insightful Questions
Prepare thoughtful questions about GSK's approach to patient safety and their R&D culture. This not only shows your interest in the company but also gives you a chance to assess if their values align with yours. Remember, interviews are a two-way street!
