Director, Regulatory Data Office Leader

Scorpion Therapeutics; Raritan (NJ); Hybrid; USD 180,000 - 240,000; Full time

Job summary

Johnson & Johnson is seeking a senior leader to head the Regulatory Data Office, advancing data stewardship, governance, and quality across innovative medicine development. The role drives global data standards and supports regulatory transformation.

You will lead a global team of data stewards, collaborate with R&D, IT, and cross-sector partners to ensure data integrity for submissions and regulatory operations, with hybrid work in the Northeast.

Qualifications

• Bachelor’s in Science, Business, or related field.
• 10+ years in pharma/healthcare with at least 2 years in data governance or stewardship.
• Prior people management experience.

Responsibilities

• Oversee regulatory data governance policies and data quality across programs.
• Lead the Regulatory Data Hub and chair the Regulatory Data Council.
• Collaborate with R&D, IT, Data Science, and cross-sector teams to embed data standards.

Skills

Data governance

Data stewardship

Team leadership

Regulatory data standards

Education

Bachelor’s in Science, Business, or related field

Tools

Veeva Vault RIM

IDMP

SPOR

Job description

Role: Lead the global Regulatory Data Office within Johnson & Johnson's Regulatory Affairs, focusing on data stewardship, governance, and quality for innovative medicine development.

Objectives

Establish trusted, high-quality regulatory data to enhance analytics, decision-making, and regulatory transformation.

Responsibilities

oversee regulatory data governance policies, manage the Regulatory Data Hub, chair the Regulatory Data Council, and drive end-to-end data integrity across R&D and enterprise platforms like URP, MDM, and eLabeling. Collaborate with R&D, IT, Data Science, and cross-sector teams to embed data standards, support global initiatives, and enable regulatory process transformation. Lead a global team of data stewards, define data standards, and ensure compliance with global health authority requirements.

Qualifications

Bachelor’s in Science, Business, or related field; 10+ years in pharma/healthcare, with at least 2 years in data governance or stewardship roles, and prior people management experience.

Preferred

experience with regulatory systems (e.g., Veeva Vault RIM, IDMP, SPOR), digital transformation, and AI tooling in regulated environments.

High-Value

focus on regulatory data standards, compliance (IDMP, xEVMPD), governance in R&D, clinical, safety, and supply chain contexts, supporting global regulatory submissions and transformation initiatives.

Location

Hybrid roles in PA or NJ; travel not specified.