Senior Business Analyst

hace 3 semanas


Madrid, Madrid, España Mygwork A tiempo completo
Job Summary

This role is with Novartis, an inclusive employer and a member of Mygwork – the largest global platform for the LGBTQ+ business community.

We are seeking an experienced IT Business Analyst to lead business analysis activities for solutions that redefine how Novartis operates. The ideal candidate will have a strong background in Global Drug Development Regulatory Affairs and excellent communication skills.

Key Responsibilities

  • Engage with global business associates to determine requirements and deliver data-driven recommendations to improve efficiency and add value.
  • Analyze the business domain and author business requirements.
Coordinate and facilitate ongoing reviews of business processes.

  • Ensure consistency and traceability between user requirements, functional specifications, and testing & validation.
Support the validation and testing as appropriate.

  • Flag issues/changes/risks to the Project Manager and workstream leads.
Work together with a product squad in delivering the Product's roadmap.

  • Liaise with vendor, Novartis internal IT teams, and business to ensure documentation is at the appropriate level of detail and that the requirements are accurately interpreted and implemented.
  • Act as an interface between business and Implementation partners.
Review the sprint demos and ensure that gaps are documented.

Requirements
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. Must have proven strong knowledge of SDLC, Validation & Compliance. Proficiency with tools such as Jira, Confluence, HPQC, Business process modelling 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).
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