Director - ABPI Signatory and Medical Reviewer
Director - ABPI Signatory and Medical Reviewer

Director - ABPI Signatory and Medical Reviewer

Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead medical governance and ensure compliance with ABPI standards in engaging healthcare professionals.
  • Company: Join GSK, a global biopharma leader dedicated to advancing health.
  • Benefits: Hybrid working model, career growth opportunities, and a supportive culture.
  • Why this job: Shape healthcare engagement while making a real impact on patient outcomes.
  • Qualifications: Registered UK medical practitioner or pharmacist with ABPI signatory experience.
  • Other info: Collaborative environment with opportunities for mentorship and professional development.

The predicted salary is between 43200 - 72000 £ per year.

Global ABPI Director Oncology

You will provide expert medical and content governance for materials and activities that engage healthcare professionals, patients, and the public. You will act as an ABPI subject matter expert, reviewing and certifying materials to ensure they meet the ABPI Code and GSK standards. You will work across functions and regions, building practical solutions to reduce regulatory risk. We value clear decision-makers who communicate kindly, coach others, and focus on high-quality, patient-centred outcomes. This role offers career growth, broad cross-functional exposure, and the chance to shape how we engage externally while supporting 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:

  • Review and certify promotional and non-promotional external materials and activities for compliance with the ABPI Code and GSK policies.
  • Provide timely, pragmatic advice to cross-functional teams on applying the ABPI Code to content, events, and external engagements.
  • Lead responses to inter-company queries, ABPI challenges, and PMCPA complaints, working closely with Legal and Compliance.
  • Design and deliver ABPI capability building for signatories and content owners to promote consistent and practical application.
  • Identify themes, risks and improvement opportunities and drive changes to processes or tools to enhance quality and compliance.
  • Act as a senior reviewer and mentor for the medical review team, supporting capability development and consistent decision-making.

Responsibilities

  • Certify materials and activities as an accredited ABPI signatory or provide final medical review where appropriate.
  • Maintain up-to-date knowledge of the ABPI Code, PMCPA decisions and other relevant guidance, and communicate implications clearly to stakeholders.
  • Collaborate with Legal, Compliance, Commercial and Medical colleagues to balance commercial objectives with regulatory and ethical obligations.
  • Support escalation processes and participate in cross-functional forums to resolve complex regulatory issues.
  • Contribute to the development of standard operating procedures, templates and checklists to improve review quality and efficiency.
  • Foster constructive working relationships across regions to ensure consistent global application of UK standards where relevant.

Why You?

Basic Qualification

  • Registered UK medical practitioner (GMC) or registered UK pharmacist (GPhC), or eligible for registration without additional examinations.
  • Accredited and experienced ABPI signatory with demonstrated use of the ABPI Code in practice.
  • Experience in a medical review, content governance or compliance role within the pharmaceutical industry.
  • Proven track record handling ABPI-related complaints or PMCPA matters.
  • Strong written and verbal communication skills, with ability to summarise complex issues clearly.
  • Comfortable working in a matrix environment and making timely, evidence-based decisions under pressure.

Preferred Qualification

  • If you have the following characteristics, it would be a plus:
  • Additional qualification in law, ethics, compliance or governance.
  • Experience designing and delivering ABPI-related training or capability programmes.
  • Experience in global or regional medical affairs or content governance teams.
  • Leadership or people management experience, including coaching and mentoring.
  • Strong analytical skills and careful attention to detail.
  • Experience working across specialty area of oncology.

Working Pattern

This role is based in the United Kingdom. It follows a hybrid working model with an expectation of regular time onsite. Exact hybrid arrangements will be discussed during the hiring process.

Closing Date for Applications: 11/02/2026

Important notices

Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements. The information that you have provided in your cover letter and CV will be used to assess your application.

Why GSK?

Uniting science, technology and talent to get ahead of disease together. 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.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call. Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive.

Director - ABPI Signatory and Medical Reviewer employer: GlaxoSmithKline

GSK is an exceptional employer, offering a dynamic work environment in the heart of London that fosters innovation and collaboration. With a strong commitment to employee growth, GSK provides ample opportunities for career advancement and professional development, all while maintaining a culture that prioritises patient-centred outcomes and ethical practices. The hybrid working model allows for flexibility, ensuring that employees can thrive both personally and professionally as they contribute to meaningful healthcare solutions.
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Contact Detail:

GlaxoSmithKline Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Director - ABPI Signatory and Medical Reviewer

✨Tip Number 1

Network like a pro! Reach out to your connections in the industry, especially those who work at GSK or have experience with ABPI. A friendly chat can open doors and give you insider info on the role.

✨Tip Number 2

Prepare for the interview by brushing up on the ABPI Code and recent PMCPA decisions. Show us you know your stuff and can apply it practically. We love candidates who can think on their feet!

✨Tip Number 3

Practice your communication skills! You’ll need to summarise complex issues clearly, so get comfortable explaining your thoughts. Mock interviews with friends can help you nail this.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we’re all about making the process smooth and straightforward for you.

We think you need these skills to ace Director - ABPI Signatory and Medical Reviewer

ABPI Code Compliance
Medical Review Expertise
Content Governance
Regulatory Knowledge
Cross-Functional Collaboration
Strong Written and Verbal Communication
Analytical Skills
Attention to Detail
Problem-Solving Skills
Leadership and Mentoring
Training and Capability Development
Experience in Oncology
Decision-Making Under Pressure
Knowledge of PMCPA Regulations

Some tips for your application 🫡

Tailor Your Cover Letter: Make sure to customise your cover letter for this role. Highlight your experience with the ABPI Code and how it aligns with the responsibilities mentioned in the job description. We want to see how you can bring your unique skills to our team!

Showcase Your Expertise: In your CV, emphasise your qualifications as a registered UK medical practitioner or pharmacist, and any relevant experience in medical review or compliance. We’re looking for clear evidence of your expertise, so don’t hold back!

Be Clear and Concise: When describing your experiences, keep it straightforward and to the point. Use bullet points where possible to make it easy for us to read. Remember, clarity is key, especially when summarising complex issues.

Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your materials and ensures you’re considered for the role. Plus, it helps us keep everything organised!

How to prepare for a job interview at GlaxoSmithKline

✨Know Your ABPI Code Inside Out

As a potential Director, it's crucial to have a solid grasp of the ABPI Code. Brush up on its key points and be ready to discuss how you've applied it in your previous roles. This will show that you’re not just familiar with the code but can also navigate its complexities effectively.

✨Showcase Your Leadership Skills

This role involves mentoring and guiding others, so be prepared to share examples of how you've led teams or projects in the past. Highlight your coaching style and how you’ve helped others develop their skills, especially in compliance and content governance.

✨Prepare for Cross-Functional Collaboration

You’ll be working closely with various teams, so think about times when you’ve successfully collaborated across functions. Be ready to discuss how you balance commercial objectives with regulatory obligations, and provide specific examples of how you’ve navigated complex situations.

✨Communicate Clearly and Confidently

Strong communication skills are essential for this role. Practice summarising complex issues in a clear and concise manner. During the interview, aim to articulate your thoughts confidently, ensuring you convey your expertise without overwhelming your audience with jargon.

Director - ABPI Signatory and Medical Reviewer
GlaxoSmithKline
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  • Director - ABPI Signatory and Medical Reviewer

    Full-Time
    43200 - 72000 £ / year (est.)
  • G

    GlaxoSmithKline

    5000-10000
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