REQ-10077741
May 20, 2026
LOC_GB

About the Role

Key Responsibilities

  • Partner with stakeholders to gather, validate and maintain accurate and complete submission planning information within operational planning tools.
  • Collaborate across Regulatory Operations, including Submission Managers, Publishers, leadership and Development Unit stakeholders, to support effective and timely resource allocation.
  • Contribute to the optimisation of resource assignment processes by implementing and supporting efficient workflows, tools and continuous improvements.
  • Apply working knowledge of global submission types, dossier components and publishing requirements to inform planning activities.
  • Ensure balanced and prioritised allocation of submission resources in line with portfolio needs and organisational priorities.
  • Develop, maintain and deliver standard resource planning metrics and insights to support leadership decision-making.
  • Support and contribute to key initiatives related to resource planning, reporting and operational excellence.

Essential Requirements

  • Demonstrated experience supporting resource planning and capacity management activities in a complex environment.
  • Strong analytical skills with the ability to interpret, manage and present data effectively.
  • Proven ability to coordinate and collaborate with stakeholders across a matrix organisation.
  • Proficiency in using resource planning tools, systems and related technologies.
  • Ability to manage multiple priorities simultaneously while maintaining a high level of accuracy and attention to detail.

Desirable Requirements

  • Demonstrates knowledge of regulatory, pharmaceutical and/or operational environments.
  • Experience working within project or resource allocation environments, including relevant tools or systems.
  • Ability to support forecasting activities and scenario planning to inform resource decisions.
  • Continuous improvement mindset with a focus on enhancing processes and operational efficiency.
  • Relevant certifications (e.g. PMP, Lean or similar) are advantageous.

Commitment to Diversity and Inclusion / EEO paragraph 

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

    Role Requirements

    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)

    DIV_GD
    Development
    LOC_GB
    London (The Westworks)
    FCT_RD
    Full time
    Regular
    No
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    REQ-10077741

    Global Regulatory Affairs Operations Resource Planner

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