Director, Clinical Data Transparency

Johnson & Johnson

Confirmed live today Low trust

Hybrid

Quick summary

Work type: Hybrid
Location: Raritan, NJTitusville, NJSpring House, PABeerse, Flemish Brabant, BelgiumLeiden, South Holland, NetherlandsHigh Wycombe, Buckinghamshire, United KingdomAllschwil, Basel-Landschaft, Switzerland
Salary: $150,000–$258,750 / yr
Posted: 2 days ago
Freshness: Confirmed live today
Closes: Oct 18, 2026
Nearby: 99+ roles within 25 mi

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $202k

This role $204k

$135k most similar roles pay here $273k

This role pays more than 50% of similar roles. Most pay $162,000–$241,534 — the shaded band above. At the midpoint, this role pays about $204k versus about $202k for comparable roles.

Based on 240 similar postings.

Employer

About Johnson & Johnson

Johnson & Johnson is a multinational corporation operating in three main segments: consumer health products, pharmaceuticals, and medical devices, known for brands like Tylenol, Band-Aid, and Janssen. Industry: Pharmaceuticals & Medical Devices

Johnson & Johnson currently has 73 open roles on FindRole.

Listed pay typically runs $109,000–$177,100 across 68 roles with salary data.

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At a glance

TL;DR · Director, Clinical Data Transparency

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Dir., Clinical Data Transparency, EHDS joins the Clinical Data Transparency business to provide strategic and operational leadership for the European Health Data Space program. This role is responsible for defining the program strategy, governance, operating model, and implementation roadmap while translating complex regulatory requirements into sustainable business capabilities. The individual will lead a cross-functional team across legal, privacy, technology, and regulatory affairs to manage integrated plans, risk mitigation, and resource planning. Key responsibilities include overseeing data inventory, change management, and executive reporting to ensure alignment with clinical data transparency goals. Required competencies include expert program and portfolio management, strategic thinking, and the ability to navigate complex stakeholder landscapes. The role requires proficiency in managing large-scale programs within the EU regulatory environment, specifically addressing challenges related to GDPR, clinical trial transparency, and data governance for innovative medicine.

Skills

Program Management Portfolio Management Agile SAFe PMP PRINCE2 Data Governance Data Management GDPR Clinical Data Transparency Database Management Information Security Risk Management Advanced Analytics Change Management Risk Management Resource Planning

What you'll do

Define and deliver the EHDS strategy, governance, operating model, and implementation roadmap based on regulatory requirements.
Lead a cross-functional program involving Legal, Privacy, Regulatory Affairs, Technology, and Data Transparency teams.
Manage the integrated program plan, including milestones, risk mitigation, resource planning, and performance tracking.
Navigate complex stakeholder landscapes to drive alignment on scope, priorities, and communication between business and technology units.
Develop executive reporting and materials to provide leadership with visibility into risks, decisions, and project status.
Oversee the change management strategy, including impact assessment, training, and transition to business-as-usual operations.
Manage external vendors and partners to ensure deliverables align with program objectives and contractual expectations.
Build scalable program management capabilities by establishing standardized tools, methods, and ways of working.

What we're looking for

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.
Substantial leadership of large, complex, cross-functional programs in a global matrix environment.
Expert program and portfolio management capability including risk management, resource planning, and executive reporting.
Formal project or program management certification such as PMP, PRINCE2, Agile, or SAFe (preferred).
Working knowledge of the EU regulatory environment and data-related obligations.
Familiarity with EHDS, GDPR, clinical trial transparency, data governance, or regulated technology implementation (strongly preferred).
Excellent communication skills to translate regulatory and technical complexity into clear executive-level messages.

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