At a Glance
- Tasks: Lead clinical audits across Europe, the Middle East and Africa to enhance patient safety.
- Company: Join GSK, a global biopharma company with a mission to impact 2.5 billion lives.
- Benefits: Competitive salary, bonuses, remote work options, and career growth opportunities.
- Other info: Flexible working culture with opportunities for professional development.
- Why this job: Make a real difference in healthcare while advancing your career in a dynamic environment.
- Qualifications: Bachelor’s degree in Life Science or related field; experience in clinical trials and audits.
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.
Position Summary
You will lead the regional audit function across Europe, the Middle East and Africa. You will design and deliver a risk-based clinical audit programme that protects patients and strengthens business performance. You will work closely with local teams, central functions and third parties to drive simple, effective controls and improvement. We value collaborative leaders who coach teams, use clear judgment and make practical decisions. This role offers visible impact, career growth and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career.
These responsibilities include some of the following:
- Lead design and delivery of a clinical risk-based audit programme across Europe, the Middle East and Africa that meets regulatory authority requirements leveraging different and novel audit types.
- Build, lead and coach a team of auditors to deliver consistent, high-quality audits and effective follow-up.
- Provide strategic input in the development, management, and implementation of strategies and initiatives, policies and procedures to support the audit program.
- Build and maintain beneficial working relationships with internal and external customers and across the Matrix in R&D Quality and Risk Management.
- Interpret metrics, trend reporting and insights to inform risk priorities and improve controls.
- Support inspection readiness, regulatory interactions and investigations of significant compliance issues.
Working pattern and location
This role is based in the United Kingdom or Poland with remote working. The role requires limited international travel.
Why You?
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelor’s degree in Life Science, Pharmacy, Health Science, or related discipline (or equivalent experience).
- Scientific/pharmaceutical industry background with experience in clinical trials.
- Knowledge of global, regional, and national regulatory requirements and regulations.
- Experience delivering risk-based audits of internal operations and third-party suppliers.
- Experience leading and developing audit teams across multiple locations.
- Project management skills and management of complex cross-functional activities.
- Verbal, written, and presentation skills and ability to influence and negotiate with senior stakeholders.
- Ability to work independently and make decisions with minimal supervision.
- Interpersonal skills, and ability to work in the matrix across geographical and organisational boundaries.
Preferred Qualification
If you have the following characteristics, it would be a plus:
- Experience supporting regulatory inspections and inspection readiness activities.
- Knowledge of GCP practices and international regulatory standards.
- Familiarity with audit management systems and data analytics tools for insight generation.
- Digital savviness - experience with AI/ML and data analytics.
- Ability to lead change, simplify processes and build trusted stakeholder relationships.
What You Will Bring
You are a practical and approachable leader who makes clear decisions. You speak plainly and listen actively. You help others grow and welcome different perspectives. You focus on simple, sustainable solutions and use evidence to guide action. You hold teams to high standards while supporting wellbeing and inclusion.
Skills
- Business Partner Relations
- Change Management
- Clinical Trials
- Continuous Improvement
- Digital Fluency
- GCP Auditing
- Problem Solving
- Quality by Design
- Risk Analysis
- Risk Management
- Stakeholder Management
- Team Leadership
Application end date: Sunday, 16 August, 2026 - EOD CET
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.
Regional Clinical Audit Director EMEA in London employer: Gsk
GSK is an exceptional employer located in Greater London, offering a dynamic and inclusive work environment that fosters innovation and collaboration. As a Senior FinOps Product Manager, you will have the opportunity to drive impactful projects while benefiting from robust employee growth opportunities and a culture that values diverse perspectives. With a commitment to professional development and a focus on agile methodologies, GSK empowers its employees to thrive in their careers while contributing to meaningful advancements in cloud financial management.
StudySmarter Expert Advice🤫
We think this is how you could land Regional Clinical Audit Director EMEA in London
✨Get Involved with Local Health Initiatives
Join local community health events or volunteer for organisations like public health agencies. This not only builds your experience but also helps you network with industry professionals who might know of openings at places like Gsk.
✨Tap into Professional Associations
Check out associations like the Institute of Healthcare Management. They often have job boards, networking events, and conferences that are perfect for connecting with potential employers in health sciences administration.
✨Stay Updated with Industry Trends
Follow health policy news and trends—being knowledgeable about the current landscape will not only help you in interviews but also make you stand out as a candidate. You can discuss recent developments and their implications when chatting with folks at Gsk.
✨Apply Through Our Website for Better Visibility
When you find roles that excite you, especially at places like Gsk, don’t forget to apply through our website. This can sometimes give you an edge by showing the employer you’re savvy and committed to finding the right fit.
We think you need these skills to ace Regional Clinical Audit Director EMEA in London
Some tips for your application 🫡
Highlight Your Relevant Experience:When applying for a role in health sciences administration, it's super important to spotlight any relevant experience you have in healthcare settings. Whether you've worked in a hospital, a clinic, or any related environment, make sure to detail those roles in your CV – focusing on your responsibilities and achievements that align with the job at Gsk.
Showcase Your Administrative Skills:Administrative skills are key in this field, so don’t hold back! Make sure your CV reflects your proficiency in things like scheduling, data management, and compliance with health regulations. Mention specific software you’ve used, such as patient management systems, as this will demonstrate your hands-on abilities and readiness for the role at Gsk.
Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to Gsk. Share a bit about why you’re drawn to this sector, any impactful situations or challenges you’ve encountered, and how they’ve shaped your desire to work in health sciences administration. This personal touch can really set you apart!
Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at Gsk. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.
How to prepare for a job interview at Gsk
✨Showcase Your Administrative Skills
In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.
✨Know Your Regulations
Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.
✨Prepare for Scenario Questions
Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.
✨Align Your Goals with the Organisation
As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research Gsk’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!
