Global Regulatory Data & Submissions Leader

Biopharma Careers; Cambridge; On-site; GBP 140,000 - 190,000; Full time

Benefits offered by this job

Health insurance

Pension scheme

Flexible working

24 days annual leave

Job summary

Sandoz is seeking a Head of Regulatory Data Management & Support to lead global data governance and regulatory data operations across product lifecycles. You’ll drive end-to-end management of xEVMPD, PMS, IDMP, CPPs, and Health Authority correspondence, ensuring accuracy, timeliness and audit-ready records in a fast-paced, cross-functional environment.

The role demands 20+ years in regulatory operations with deep knowledge of regulatory data models, Veeva ecosystems, and digital

Qualifications

• Minimum: Degree or equivalent work experience.
• Fluent English required (oral and written).
• Expert knowledge of regulatory affairs with end-to-end processes and data flows.

Responsibilities

• Lead Regulatory Data Governance and Quality across global datasets.
• Direct end-to-end xEVMPD and PMS data management and submissions.
• Oversee Health Authority correspondence management and CPP/document workflows.
• Collaborate with Regulatory Affairs, Safety, CMC, Quality, Supply Chain, and IT for data consistency and automation.

Skills

Fluent English

Regulatory operations leadership

Regulatory data governance

Veeva systems knowledge

Data quality governance

Education

Degree or equivalent

Tools

Veeva Vault

RIMS

AI/Automation tools

Job description

Sandoz is seeking a Head of Regulatory Data Management & Support to lead global data governance and regulatory data operations across product lifecycles. You’ll drive end-to-end management of xEVMPD, PMS, IDMP, CPPs, and Health Authority correspondence, ensuring accuracy, timeliness and audit-ready records in a fast-paced, cross-functional environment.

The role demands 20+ years in regulatory operations with deep knowledge of regulatory data models, Veeva ecosystems, and digital