Senior Business Consultant

hace 2 semanas

Barcelona, Barcelona, España Advanced Accelerator Applications (Italy) - S... A tiempo completo

Job Summary

This role is responsible for acting as a consultant and advisor to improve complex global business processes, products, and services. The ideal candidate will have experience in Global Drug Development Regulatory Affairs and lead business analysis activities for solutions that redefine how the company operates.

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.
  • Actively participate in sprint planning discussions and ensure sprint functional deliverables are on track.
  • Liaise with the vendor, 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.
  • 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.
  • Experience in Managing GxP Projects and Related Fields is a plus.

Benefits

  • Company Pension plan.
  • Life and Accidental Insurance.
  • Meals.
  • Allowance or Canteen in the office.
  • Flexible working hours.

Commitment to Diversity & Inclusion

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

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