Dir., Clinical Data Transparency, EHDS

Scorpion Therapeutics; New Jersey; Hybrid; USD 140,000 - 200,000; Full time

Job summary

Johnson & Johnson is seeking a leader to steer the European Health Data Space program within Clinical Data Transparency, aligning regulatory, technical, and business requirements to deliver a compliant, scalable data governance framework.

You will coordinate cross-functional teams across regulatory, legal, technology, and business units, manage risks, and drive change management with a hybrid work model across Europe and the US.

Qualifications

• Advanced degree in science, healthcare, technology, or business.
• At least 7 years of experience leading pharmaceutical/healthcare/scientific programs.
• Expertise in global regulatory environments, data governance, and technology implementation.
• PMP, PRINCE2, Agile, or SAFe certification preferred.

Responsibilities

• Define and deliver the EHDS strategy.
• Build governance frameworks.
• Oversee cross-functional program planning and execution.
• Manage stakeholder alignment.
• Mitigate risks.
• Ensure technology and change management plans are implemented.

Skills

Regulatory knowledge

Program leadership

Stakeholder management

Risk management

Global regulatory experience

Data governance

Technology implementation

Education

Advanced degree (science/health/tech/business)

Tools

PMP certification

PRINCE2 certification

Agile

SAFe

Job description

Role:

Lead the strategic and operational execution of Johnson & Johnson's European Health Data Space (EHDS) program within the Clinical Data Transparency division, focusing on integrating regulatory, technological, and business requirements.

Responsibilities:

define and deliver the EHDS strategy, build governance frameworks, oversee cross-functional program planning and execution, manage stakeholder alignment, mitigate risks, and ensure technology and change management plans are effectively implemented.

Requirements:

advanced degree in science, healthcare, technology, or business; at least 7 years of experience in pharmaceutical, healthcare, or scientific program leadership; expertise in global regulatory environments, data governance, and technology implementation; PMP, PRINCE2, Agile, or SAFe certification preferred.

High-Value:

complex multi-country program management, EU data regulations including GDPR, clinical data transparency, cross-functional leadership across regulatory, legal, technology, and business units, with hybrid work model in Belgium, Netherlands, UK, Switzerland, or US.

Collaboration involves external vendors, industry groups, and internal senior leadership.

Travel may be required.

The role emphasizes strategic planning, governance, stakeholder management, and program delivery within a regulated biopharma context.