Director, European Health Data Space (EHDS) Programme

7555-Janssen Pharmaceutica NV Legal Entity; Geel; Hybride; EUR 119 000 - 204 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Flexible working environment

Career development opportunities

Employee benefits

Résumé du poste

Johnson & Johnson seeks a Director to lead the European Health Data Space (EHDS) Programme within its Clinical Data Transparency team. You will translate regulatory requirements into sustainable capabilities and manage a cross‑functional program spanning Global Development, Legal, Privacy, Regulatory Affairs, Technology, and Data Transparency.

You will set strategy, governance, and an integrated delivery plan, directing workstreams, managing risks and dependencies, and reporting progress to

Qualifications

• Advanced degree in a scientific, technology, healthcare, or business discipline, or equivalent experience.
• At least 7 years of relevant pharmaceutical, healthcare, technology, or scientific experience.
• Formal project or program management certification, such as PMP, PRINCE2, Agile, or SAFe, is preferred.
• Working knowledge of EU regulatory environment; familiarity with EHDS, GDPR, data governance, or regulated technology implementation is preferred.

Responsabilités

• Leads EHDS strategy, governance, operating model, and implementation roadmap across multiple functions.
• Directs program execution, governance, reporting, and risk/issue management.
• Partners with senior stakeholders, drives alignment on scope, priorities, and sequencing.
• Oversees resource planning, external partnerships, and transition to business-as-usual operations.
• Creates executive communications and ensures successful program delivery and adoption.

Connaissances

Strategic program leadership

Regulatory knowledge

Stakeholder management

Excellent communication

Formation

Advanced degree in scientific/tech/healthcare or business

Description du poste

Johnson & Johnson seeks a Director to lead the European Health Data Space (EHDS) Programme within its Clinical Data Transparency team. You will translate regulatory requirements into sustainable capabilities and manage a cross‑functional program spanning Global Development, Legal, Privacy, Regulatory Affairs, Technology, and Data Transparency.

You will set strategy, governance, and an integrated delivery plan, directing workstreams, managing risks and dependencies, and reporting progress to