About the Role
As a Medical Affairs Pharmacist, you will combine your clinical expertise with a strong understanding of regulatory and compliance requirements. You will support the design of therapy review services and ensure that materials and processes meet all applicable industry codes, legislation, and quality standards.
A key part of the role is ensuring compliance with the Association of the British Pharmaceutical Industry Code of Practice, which governs interactions between pharmaceutical companies, healthcare professionals, and healthcare organisations in the United Kingdom.
This is an office‑based role with flexible working, where most of the team operates remotely while staying closely connected through regular collaboration.
What You Will Be Doing
1. Developing, maintaining, and updating written materials for clinical services, including service protocols and supporting documents
2. Ensuring that all materials comply with the Association of the British Pharmaceutical Industry Code of Practice, data protection requirements, and relevant clinical guidance
3. Supporting submission and approval processes by working closely with internal stakeholders and external client approval teams
4. Acting as a subject matter expert on compliance matters related to clinical services
5. Supporting pharmacovigilance activities, including reporting processes and related documentation
6. Facilitating and supporting training on pharmacovigilance, information governance, and industry codes of practice
7. Collaborating with teams across Medical Affairs, Service Design, Marketing, Project Management, and Account Management
8. Keeping up to date with changes in legislation, regulatory requirements, and clinical guidelines relevant to service delivery
9. Promoting a culture of integrity, openness, and continuous improvement
What We Are Looking For
10. Qualified pharmacist
11. Strong attention to detail and a structured, organised approach to work
12. Experience or familiarity with the Association of the British Pharmaceutical Industry Code of Practice
13. Confidence working with internal and external stakeholders, including clients
14. Ability to manage multiple priorities and projects effectively
15. Interest in working in a medical affairs, compliance, or service design environment
16. Experience with pharmacovigilance activities is an advantage
Why Join IQVIA
IQVIA is a global leader in healthcare intelligence, technology, and research. We offer a collaborative working environment, flexible working arrangements, and opportunities to develop your career across a wide range of healthcare and life sciences disciplines.
You will be part of a team that values expertise, integrity, and impact, and you will contribute to services that support healthcare professionals and improve patient care.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.