At a Glance
- Tasks: Lead safety evaluations and risk management strategies in oncology.
- Company: Join a global pharmaceutical leader committed to patient safety.
- Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with mentorship opportunities and a focus on continuous improvement.
- Why this job: Make a real impact on patient safety while advancing your career.
- Qualifications: Bachelor's in health sciences; experience in pharmacovigilance or drug safety.
The predicted salary is between 80000 - 100000 € per year.
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
Working Pattern
This role is based in the United Kingdom and operates on a hybrid working model with an agreed mix of office and remote work to support collaboration and governance activities.
How to 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.
Equal Employment Opportunity
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.
Adjustments
Contact UKRecruitment.Adjustments@gsk.com
SERM Scientific Director, Oncology employer: GlaxoSmithKline
GSK is an exceptional employer, offering a dynamic work culture that prioritises collaboration and innovation in the field of patient safety. With a hybrid working model based in the UK, employees benefit from flexible working arrangements while being part of a global team dedicated to meaningful impact and professional growth opportunities. The company fosters an inclusive environment where diverse talents are valued, ensuring that every team member can thrive and contribute to advancing healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land SERM Scientific Director, Oncology
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work in pharmacovigilance or oncology. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of global pharmacovigilance regulations. We want you to be able to discuss how you can contribute to safety evaluations and risk management strategies confidently.
✨Tip Number 3
Showcase your leadership skills! If you've mentored or led teams before, make sure to highlight these experiences during interviews. We love candidates who can inspire others in a matrix environment.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you're serious about joining our global safety team.
We think you need these skills to ace SERM Scientific Director, Oncology
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 leadership roles you've had. We want to see how your background aligns with our needs!
Craft a Compelling Note:When writing your short note, be genuine! Share what you can bring to the role and what you hope to learn. This is your chance to show us your passion for patient safety and your eagerness to grow within our global safety team.
Showcase Your Data Skills:Since analysing complex data is key for this role, make sure to mention any relevant experiences where you've successfully communicated findings to diverse stakeholders. We love seeing how you can turn data into actionable insights!
Apply Through Our Website:Don’t forget 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 shows you’re serious about joining our team at StudySmarter!
How to prepare for a job interview at GlaxoSmithKline
✨Know Your Stuff
Make sure you brush up on pharmacovigilance and risk management strategies. Familiarise yourself with global regulations like ICH and GVP, as well as the latest trends in oncology safety. This will help you speak confidently about your expertise and how it aligns with the role.
✨Showcase Your Leadership Skills
Since this role may involve mentoring or leading teams, be prepared to discuss your experience in cross-functional environments. Share specific examples of how you've influenced projects or guided colleagues, highlighting your ability to collaborate effectively.
✨Prepare for Data Discussions
You’ll likely need to analyse complex safety data, so practice explaining your findings clearly. Think of a few scenarios where you’ve had to assess safety signals and implement mitigation strategies, and be ready to walk the interviewers through your thought process.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company’s approach to patient safety and regulatory interactions. This not only demonstrates your enthusiasm but also gives you a chance to gauge if the company culture aligns with your values.
