At a Glance
- Tasks: Lead safety evaluations and risk management strategies in oncology.
- Company: Join a global leader in pharmaceuticals committed to patient safety.
- Benefits: Competitive salary, diverse work environment, and opportunities for professional growth.
- Other info: Collaborative culture with mentorship opportunities and a focus on continuous improvement.
- Why this job: Make a real impact on patient safety and contribute to innovative healthcare solutions.
- Qualifications: Bachelor's in health sciences; experience in pharmacovigilance or drug safety required.
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.
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 elevate 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.
Qualifications
- 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.
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.
SERM Scientific Director, Oncology employer: Gsk
GSK is an exceptional employer, offering a dynamic work environment that fosters collaboration and innovation in the field of oncology. With a strong commitment to employee growth, GSK provides ample opportunities for professional development and mentorship within a global framework, ensuring that every team member can contribute meaningfully to patient safety and product excellence. Located in a vibrant area, employees benefit from a supportive culture that values diversity and inclusion, making it an ideal place for those seeking a rewarding career in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land SERM Scientific Director, Oncology
✨Network Like a Pro
Get out there and connect with folks in the industry! Attend conferences, webinars, or local meet-ups related to pharmacovigilance and oncology. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Show Off Your Expertise
When you get the chance to chat with potential employers, make sure to highlight your experience in safety evaluation and risk management. Share specific examples of how you've tackled safety concerns or contributed to regulatory submissions – it’ll show you mean business!
✨Be Ready for the Interview
Prepare for those tricky interview questions by brushing up on global pharmacovigilance regulations and guidelines. Think about how you can demonstrate your ability to analyse complex data and communicate findings clearly – that’s what they want to hear!
✨Apply Through Our Website
Don’t forget to check out our website for the latest job openings! Applying directly through us not only shows your interest but also gives you a better chance of being noticed by the hiring team. Let’s land that dream job together!
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 mention any leadership roles you've had in cross-functional teams.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about patient safety and how your background aligns with our mission at StudySmarter. Be specific about your achievements in drug safety.
Showcase Your Analytical Skills:Since this role involves analysing complex data, make sure to include examples of how you've successfully interpreted safety data in past positions. We want to see your thought process and decision-making skills!
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status directly!
How to prepare for a job interview at Gsk
✨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 specific safety concerns related to oncology. This will help you demonstrate your expertise and show that you're ready to lead in this role.
✨Showcase Your Leadership Skills
Since this position may involve mentoring or leading teams, be prepared to discuss your previous leadership experiences. Think of examples where you've successfully influenced cross-functional teams or contributed to regulatory submissions. Highlighting these experiences will show that you can thrive in a matrix environment.
✨Communicate Clearly
You’ll need to analyse complex data and communicate findings to diverse stakeholders. Practice explaining technical concepts in simple terms. During the interview, focus on how you would convey safety information effectively to both scientific and non-scientific audiences.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past situations where you identified safety signals or implemented mitigation strategies. Be ready to walk the interviewer through your thought process and decision-making steps.
