Director - ABPI Signatory and Medical Reviewer in London
Director - ABPI Signatory and Medical Reviewer

Director - ABPI Signatory and Medical Reviewer in London

London Full-Time 36000 - 60000 ÂŁ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead medical governance and ensure compliance for engaging healthcare professionals and the public.
  • Company: Join GSK, a global leader in healthcare innovation.
  • Benefits: Hybrid working model, career growth, and opportunities to shape healthcare engagement.
  • Why this job: Make a real impact in oncology while supporting ethical standards in healthcare.
  • Qualifications: Registered UK medical practitioner or pharmacist with ABPI signatory experience.
  • Other info: Collaborative environment with strong focus on professional development.

The predicted salary is between 36000 - 60000 ÂŁ per year.

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. 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.

Key Responsibilities

  • 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.

Basic Qualifications

  • 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 Qualifications

  • 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 and follows a hybrid working model with an expectation of regular time onsite. Exact hybrid arrangements will be discussed during the hiring process.

Application

Closing Date for Applications: 11/02/2026. 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.

Equal Opportunity Employer

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.

Support for Applicants

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.

Director - ABPI Signatory and Medical Reviewer in London employer: Gsk

GSK is an exceptional employer, offering a dynamic work environment that fosters collaboration and innovation in the healthcare sector. With a strong commitment to employee growth, you will have access to extensive training and development opportunities, particularly in the field of oncology, while working within a supportive hybrid model that promotes work-life balance. Join us to make a meaningful impact on patient engagement and compliance, all while being part of a diverse team dedicated to advancing science and technology.
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Contact Detail:

Gsk Recruiting Team

StudySmarter Expert Advice 🤫

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

✨Tip Number 1

Network like a pro! Reach out to professionals in the oncology field, especially those who are already working at GSK or similar companies. A friendly chat can open doors and give you insider info on the role.

✨Tip Number 2

Prepare for interviews by brushing up on the ABPI Code and recent PMCPA decisions. Being able to discuss these topics confidently will show that you're not just a candidate, but a knowledgeable expert ready to contribute.

✨Tip Number 3

Showcase your leadership skills! If you've mentored others or led projects, make sure to highlight these experiences. GSK values collaboration and guidance, so let them know how you can support their teams.

✨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 family and contributing to their mission.

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

ABPI Code Compliance
Medical Review Expertise
Content Governance
Regulatory Risk Management
Cross-Functional Collaboration
Legal and Compliance Knowledge
Training and Capability Development
Analytical Skills
Attention to Detail
Strong Written and Verbal Communication
Matrix Environment Experience
Leadership and Mentoring
Oncology Knowledge
Problem-Solving Skills

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 relates to the responsibilities listed in the job description. We want to see how you can bring your unique skills to our team!

Showcase Your Experience: In your CV, focus on your relevant experience in medical review and content governance. Use specific examples that demonstrate your ability to handle ABPI-related complaints or PMCPA matters. This will help us understand your background better.

Be Clear and Concise: When writing your application, clarity is key! Summarise complex issues clearly and avoid jargon where possible. We appreciate straightforward communication, especially in a role that requires strong written skills.

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’s super easy to do!

How to prepare for a job interview at Gsk

✨Know Your ABPI Code Inside Out

Make sure you have a solid understanding of the ABPI Code and how it applies to the role. Brush up on recent PMCPA decisions and be ready to discuss how these impact compliance in your previous work.

✨Showcase Your Cross-Functional Experience

Prepare examples that highlight your experience working with different teams, such as Legal, Compliance, and Medical. Be ready to explain how you’ve successfully navigated complex regulatory issues in a matrix environment.

✨Demonstrate Leadership and Mentoring Skills

Since this role involves mentoring others, think of specific instances where you've led a team or trained colleagues. Share how you fostered a collaborative environment and improved decision-making processes.

✨Communicate Clearly and Confidently

Practice summarising complex issues in a clear and concise manner. During the interview, focus on articulating your thoughts effectively, as strong communication skills are crucial for this position.

Director - ABPI Signatory and Medical Reviewer in London
Gsk
Location: London

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  • Director - ABPI Signatory and Medical Reviewer in London

    London
    Full-Time
    36000 - 60000 ÂŁ / year (est.)
  • G

    Gsk

    10000+
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