Qualifications / Requirements

- Education: PhD or Master's in informatics, computer science, life sciences, or related discipline.
- Experience: 8+ years in pharma/biotech R&D; focusing on Global Regulatory Affairs, regulatory operations, regulatory technology, or data product management.
- Strong track record in data product development, integration, or semantic modelling in a regulated domain.
- Experience with multi-modal regulatory data (submission, labelling, intelligence, compliance datasets).

Skills & Expertise

- Deep knowledge of Global Regulatory Affairs processes, submission pathways (e.g., eCTD), and global health authority requirements.
- Deep knowledge of data products, database design, and data transformation/mapping.




- Familiarity with metadata management, ontologies, knowledge graphs, and industry standards (e.g., IDMP, xEVMPD, ICH, eCTD).
- Robust leadership, collaboration, and communication skills; ability to translate technical strategy into business/science value.
- Demonstrated ability to influence stakeholders and drive adoption of new data capabilities across a complex organization.

Other

- Primary location: Spring House, PA (also open to Titusville, NJ).
- Requires up to 25% travel.
- Contract type: Fixed-term contract.

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📌 Property Manager (Central US) (City of Sydney)
🏢 Global Modern Services, Inc. (Usa)
📍 City of Sydney