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Senior Business Consultant

hace 2 meses


Madrid, Madrid, España Mod It Services Gmbh A tiempo completo

Job Summary

This role is designed to provide strategic guidance and support to improve complex global business processes, products, and services. We are seeking an experienced professional in Global Drug Development Regulatory Affairs to lead business analysis activities for solutions that redefine how Novartis operates.

About the Role

The successful candidate will be responsible for:

  • Engaging with global business associates to determine requirements and deliver data-driven recommendations to improve efficiency and add value.
  • Analyzing the business domain and authoring business requirements.
  • Coordinating and facilitating ongoing reviews of business processes.
  • Ensuring consistency and traceability between user requirements, functional specifications, and testing & validation.
  • Supporting the validation and testing as appropriate.
  • Flagging issues/changes/risks to the Project Manager and workstream leads.
  • Working together with a product squad to deliver the Product's roadmap.
  • Actively participating in sprint planning discussions and ensuring sprint functional deliverables are on track.
  • Liaising with vendors, Novartis internal IT teams, and business to ensure documentation is at the appropriate level of detail and that requirements are accurately interpreted and implemented.
  • Acting as an interface between business and implementation partners.
  • Reviewing sprint demos and ensuring that gaps are documented.

Requirements

The ideal candidate will possess:

  • A Bachelor's degree in engineering or pharmaceutical discipline.
  • An advanced degree (MBA, MS, etc.) and related accreditations (IIBA, Veeva, Agile certifications, etc.) is a plus.
  • 7+ years of IT Business Analysis experience with excellent communication skills.
  • Proven strong knowledge of SDLC, Validation & Compliance.
  • Proficiency with tools such as Jira, Confluence, HPQC, Business process modeling tools.
  • Experience in Data migration and System integration related projects.
  • Multi-national global experience in interacting with senior management, collaborating across boundaries, and relationship management, and influencing without authority.
  • Experience in Regulatory Affairs business processes is a plus (e.g. Registration Management, Submission Management, Submission Content management, Submission Publishing & Clinical Publishing, Product Labelling).
  • Implementation experience of Veeva Submission and Submission Archive module is a plus.