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- Tasks: Lead safety evaluations and risk management for innovative medicines and vaccines.
- Company: Join GSK, a global biopharma leader with a mission to impact 2.5 billion lives.
- Benefits: Hybrid working model, competitive salary, and opportunities for professional growth.
- Why this job: Shape patient safety strategies and make a real difference in healthcare.
- Qualifications: Medical degree and experience in pharmacovigilance or drug safety required.
- Other info: Collaborative culture focused on innovation and patient impact.
The predicted salary is between 43200 - 72000 £ 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.
Position Summary: Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate. Makes recommendations for the further characterization, management, and communication of safety risks.
Key Responsibilities:
- Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix.
- Leads the safety component of global regulatory submissions.
- Demonstrated track record of quality decision making and creative problem resolution.
- Explores positions and alternatives to reach mutually beneficial agreements and solutions.
- Leads safety governance by development of safety strategy and its execution for products in clinical development and post marketing settings.
- Facilitates safety governance/SRTs in the clinical development and post marketing settings.
- Represents GS on cross-functional Clinical Matrix Teams and/or Project Teams.
- Authors/participates in written standard updates (e.g., SOPs).
- Builds strong working relationships and displays excellent leadership skills on safety issues.
- Leads presentations on recommendations or safety issues to senior staff members at the GSK Senior Governance Committees.
- Leads inspection readiness and prepared as needed to support audits/inspections.
Basic Qualifications:
- Medical degree
- Completion of a formal postgraduate clinical training, clinical residency or specialty training
- Advanced experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance, or Drug Safety
- Significant pharmacovigilance experience relating to Safety Evaluation and Risk Management
- Experience with Signal Detection and safety surveillance
- Knowledge/experience of international pharmacovigilance requirements
- Experience working in large matrix organizations
Preferred Qualifications:
- Experience leading cross-functional safety governance or Senior Review Teams.
- Immunology SERM background
- Experience with safety databases, safety systems configuration or validated computerized systems.
- Track record mentoring or managing scientific colleagues in safety roles.
What you will gain: You will expand your influence across global safety operations and develop skills in safety strategy, regulatory interactions and cross-functional leadership.
Working model: This role is hybrid, based in the United Kingdom. You will be expected on site for key meetings, governance activities and team collaboration.
How to apply: If this role speaks to you, please apply with your CV and a short note describing a safety assessment or risk management activity you led and its impact.
GSK is an Equal Opportunity Employer. We believe in an agile working culture for all our roles.
SERM Medical Director in London employer: GlaxoSmithKline
Contact Detail:
GlaxoSmithKline Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land SERM Medical Director in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at GSK or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by researching GSK's recent projects and initiatives. Show that you’re not just interested in the role but also passionate about their mission to impact patient health positively.
✨Tip Number 3
Practice your pitch! Be ready to explain how your experience in pharmacovigilance and risk management aligns with GSK’s goals. Keep it concise and impactful to grab their attention.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the GSK team.
We think you need these skills to ace SERM Medical Director in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the SERM Medical Director role. Highlight your relevant experience in pharmacovigilance and risk management, and don’t forget to showcase any leadership roles you've had in cross-functional teams.
Craft a Compelling Cover Note: Your cover note should be a brief but impactful summary of your experience. Describe a specific safety assessment or risk management activity you led, focusing on its impact. This is your chance to show us how you can contribute to our mission!
Showcase Your Communication Skills: Since this role involves a lot of communication, make sure your written application reflects your ability to convey complex information clearly. Use concise language and structure your thoughts logically to demonstrate your communication prowess.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at GlaxoSmithKline
✨Know Your Stuff
Make sure you brush up on your pharmacovigilance and risk management knowledge. Familiarise yourself with GSK's recent projects and how they align with patient safety. Being able to discuss specific examples will show that you're not just knowledgeable but also genuinely interested in their work.
✨Showcase Your Leadership Skills
Since this role involves leading cross-functional teams, be prepared to share examples of how you've successfully led teams in the past. Highlight your ability to influence others and manage safety issues effectively. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Prepare for Technical Questions
Expect questions that dive deep into your experience with safety databases and signal detection. Brush up on international pharmacovigilance requirements and be ready to discuss how you've applied these in your previous roles. This will demonstrate your expertise and readiness for the challenges ahead.
✨Engage with the Interviewers
Interviews are a two-way street! Prepare thoughtful questions about GSK’s approach to safety governance and how they foster collaboration within teams. This not only shows your interest but also helps you gauge if the company culture aligns with your values.
