Skip to main content
Post your CV and find your next job on Indeed!

Medical Information Officer Pharmaceutical jobs

Sort by: -
    • Significant Medical Affairs, Quality and Compliance experience within the pharmaceutical industry.
    • As Head of International Medical Affairs, Process…
    • Fulfil the responsibilities of the Responsible Person under applicable UK pharmaceutical legislation.
    • Practical experience with pharmaceutical importation and…
    • Governance & Compliance: Establish and oversee global governance frameworks, ensuring all medical activities uphold the highest ethical and scientific standards…
  • View similar jobs with this employer
    • A minimum of 10 years of Medical Affairs, Clinical Development, or related pharmaceutical or biotechnology industry experience is required, preferably in…
    • Minimum 15 years of pharmaceutical or biotechnology experience and a minimum of 10 years leading Medical Communications, Medical Affairs, Publications or…
    • Regulatory Compliance & Clinical Governance Pharmacist.
    • £65,000–£75,000 + performance bonus | Permanent, full-time | Ilford, Greater London (hybrid).
    • Remote Role | 1 Day Per Month On-Site | Competitive Day Rate.
    • We are seeking a highly credible and experienced Chief Medical Officer (CMO) to provide clinical…
    • Regulatory experience in the pharmaceutical industry minimum 5 years which includes the Preparation of modules for the regulatory dossier in eCTD format,…
    • You'll set global labelling strategy, balancing business need against the core obligation of getting benefit/risk information right for the people relying on it…
    • Lead the development of the breast cancer medical narrative by identifying and advancing key analytic needs and informing the interpretation of pivotal trial…
    • Lead the development of the breast cancer medical narrative by identifying and advancing key analytic needs and informing the interpretation of pivotal trial…
    • Provide senior medical leadership, clinical supervision and guidance to Occupational Health Physicians and wider clinical teams.
    • Experience operating in cyber security, technology, pharmaceutical, life sciences or another highly regulated environment.
    • View all GlaxoSmithKline jobs - London jobs - Senior CyberSecurity Engineer jobs in London
    • Salary Search: Senior Manager, Cyber Security Office PMO salaries in London
    • See popular questions & answers about GlaxoSmithKline
    • Significant regulatory-affairs experience across pharmaceutical development and the product lifecycle.
    • Translate complex scientific and regulatory information…
    • Provide Clinical Quality oversight and support of the clinical study teams.
    • “Seat at the table” for regular partnership level and ad hoc team meetings.

People also searched:

information manager

Job Post Details

Head of International Medical Affairs, Process Effectiveness and Monitoring
London
•
Hybrid work
£102,410 - £190,190 a year
Full-time

Job details

£102,410 - £190,190 a year
Full-time
Hybrid work in London

Full job description

Summary

#LI-Hybrid

Location: London, UK.

Relocation Support: Yes

Are you ready to strengthen how International Medical Affairs translates governance into consistent, effective execution?

As Head of International Medical Affairs, Process Effectiveness and Monitoring, you will lead the advancement of process effectiveness and monitoring across International Medical Affairs, helping ensure robust governance, proactive risk management, and sustainable operational excellence. Reporting to the Head of Medical Affairs Governance & Operations, IMA, you will work across functions and geographies to strengthen first-line monitoring, support audit and inspection readiness, and turn insights into meaningful improvements in how teams operate. This is a highly visible leadership opportunity to combine governance expertise, transformation, and digital innovation to simplify ways of working, strengthen compliance, and enable Medical Affairs teams to deliver their priorities with greater consistency and impact.

About the Role

Key Responsibilities:

  • Lead process effectiveness and first-line monitoring across International Medical Affairs to strengthen consistent, compliant execution.
  • Design and evolve monitoring frameworks that identify governance risks, trends, gaps, and opportunities for continuous improvement.
  • Translate monitoring insights into targeted corrective and preventive actions that strengthen Medical Affairs processes and ways of working.
  • Drive proactive risk management, ensuring emerging governance and compliance risks are identified, assessed, and appropriately addressed.
  • Strengthen audit and inspection readiness by embedding sustainable processes, monitoring practices, and clear accountability across International Medical Affairs.
  • Partner with country, regional, and functional stakeholders to improve process adoption, governance implementation, and operational effectiveness.
  • Lead process simplification and transformation initiatives that improve efficiency while maintaining appropriate governance and compliance standards.
  • Establish meaningful metrics and insights that enable leadership to assess process effectiveness and prioritize improvement opportunities.
  • Champion responsible use of Artificial Intelligence, analytics, and digital solutions to enhance monitoring, insights, and operational efficiency.
  • Lead, develop, and empower the Process Effectiveness and Monitoring team while building strong networks across functions and geographies.

Essential Requirements:

  • Advanced degree in Medicine, Pharmacy, Life Sciences, or a related field.
  • Significant Medical Affairs, Quality and Compliance experience within the pharmaceutical industry.
  • Proven experience in international, regional, or above-country Medical Affairs roles within a complex global organization.
  • Deep experience leading multi-country first-line assurance, including risk-based monitoring, quality oversight, internal controls, and corrective and preventive action management.
  • Strong experience translating enterprise standards into country practice, including audit and inspection readiness and cross-country remediation.
  • Experience defining performance and quality indicators, analyzing monitoring trends, and translating insights into recommendations for senior leadership.
  • Previous people leadership experience, including proven ability to lead, develop, and empower high-performing teams and build effective networks across geographies.
  • Excellent written and spoken English, with strong communication, influencing, analytical, organizational, and stakeholder-management capabilities.

Desirable Requirements:

  • Formal training or certification in Quality, Risk Management, or Compliance.
  • Proficiency in additional languages beyond English is an advantage.




Benefits: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: Novartis Life Handbook



Expected Annual Base Salary Range for role: 102,410.00 - 190,190.00 GBP



The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.


In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.


The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.


In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. Long-term equity awards granted at group level may also be part of your package. Further details will be provided during the application process.



Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.



Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)


Primary location salary range
£102,410.00 - £190,190.00
Division
International
Business Unit
General Management
Location
United Kingdom
Site
London (The Westworks)
Company / Legal Entity
GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No

Let Employers Find YouUpload Your Resume