Principal – Management Consultant, Regulatory

This is a fully remote position, open to applicants in Germany.

📋 Description

• Assume responsibility for one or multiple projects.

• Lead a project team to ensure that expectations are fulfilled.

• Introduce and implement best practices and methodologies to provide value for the client.

• Conduct workshops, gather requirements, manage vendor selection, and execute data migrations.

• Serve as the liaison between the organization and software vendors.

• Enhance business processes.

• Foster a culture of knowledge sharing.

• Identify and suggest opportunities to boost team performance.

⛳️ Requirements

• Over 5–8 years of experience in the pharmaceutical sector.

• Proficiency in Regulatory Operations and Regulatory Information Management.

• Comprehensive understanding of regulatory processes and data.

• Expertise in data management, including Data Governance and Master Data Management.

• Practical experience with xEVMPD and IDMP.

• Familiarity with relevant guidance, such as the EU IDMP Implementation Guide.

• Experience in implementing and managing RIM systems.

• Development and execution of data migration strategies.

• Strong affinity for both business and technology.

🏝️ Benefits

• Competitive compensation with bonus potential.

• Flexible working hours and opportunities for remote work.

• Access to state-of-the-art equipment for both office and remote environments.

• A creative workspace and inspiring events.

• Regular international team meetings and company gatherings.

• A secure position with long-term career prospects.