Director, Regulatory Data Office Leader

Scorpion Therapeutics; New Jersey; Hybrid; USD 140,000 - 190,000; Full time

Job summary

Scorpion Therapeutics seeks a Lead for the Regulatory Data Office within Global Regulatory Affairs to steward governance, data integrity, and decision support for regulatory submissions.

You will drive data-driven transformation across RIM and regulated data environments, partnering with R&D, IT, and Data Science to advance enterprise-wide digital solutions including AI.

Qualifications

• Bachelor’s degree required in science, business, or related field.
• 10+ years in pharma/healthcare with at least 2 years managing teams.
• Deep regulatory domain expertise and experience with data standards.

Responsibilities

• Oversee the Regulatory Data Hub and governance policies; chair the Regulatory Data Council; ensure data quality and compliance with global regulations (IDMP, SPOR).
• Drive data-driven transformation initiatives; support RIM projects; embed governance into digital solutions including AI and automation.
• Lead and develop a global team of data stewards; collaborate across R&D, IT, and Data Science.

Skills

Data governance

Leadership

Regulatory data

Cross-functional collaboration

AI tools

Education

Bachelor’s degree (Science, Business, or related)

Tools

Veeva Vault RIM

IDMP

Job description

Role:

Lead the Regulatory Data Office within Global Regulatory Affairs, focusing on data stewardship, governance, and integrity to support regulatory submissions and decision‑making.

Responsibilities:

• Oversee the Regulatory Data Hub, establish governance policies, chair the Regulatory Data Council, and ensure data quality, standards, and compliance with global regulations (e.g., IDMP, SPOR).
• Drive data‑driven transformation initiatives, support RIM projects, and embed data governance into enterprise‑wide digital solutions, including AI and automation.
• Lead and develop a global team of data stewards, fostering collaboration across R&D, IT, and Data Science.

Qualifications:

• Bachelor’s in Science, Business, or related;
• 10+ years in pharma/healthcare, with at least 2 years managing teams;
• deep regulatory domain expertise;
• experience with data standards (Veeva Vault RIM, IDMP), data governance, and regulated data environments.
• Preferred skills include knowledge of regulatory systems, digital transformation, and AI tools, along with strong leadership and cross‑functional influence capabilities.

HighValue:

global regulatory data governance, compliance with IDMP/SPOR, RIM platform expertise, cross‑functional leadership, digital transformation, and regulated data management.

WorkSetup:

hybrid in Horsham PA, Raritan NJ, or Titusville NJ.