Global Regulatory Disclosures Lead

Roche Diagnostics International Ltd.; Welwyn; On-site; GBP 45,000 - 65,000; Full time

Job summary

A leading global healthcare company in Welwyn is seeking a Regulatory Affairs Specialist to ensure compliance with global regulatory disclosures and drive transparency in clinical trial data. The ideal candidate will have a degree in Life Sciences, project management expertise, and experience in regulatory affairs. Responsibilities include managing disclosure requirements, mentoring colleagues, and leading initiatives to optimize processes. This role offers the opportunity to make a significant impact on healthcare access worldwide.

Qualifications

• Strong experience in supporting cross-functional teams in a scientific or regulatory environment.
• Proven ability to deliver high-quality work under challenging timelines.
• Extensive experience in regulatory affairs and global regulations.

Responsibilities

• Ensure compliance with global disclosure requirements while protecting sensitive information.
• Drive the accurate posting of clinical trial protocols to public registries.
• Lead initiatives to optimize information and processes.

Skills

Project management expertise

Collaboration across global teams

Excellent written and verbal communication

Education

Degree in Life Sciences or equivalent

Job description

A leading global healthcare company in Welwyn is seeking a Regulatory Affairs Specialist to ensure compliance with global regulatory disclosures and drive transparency in clinical trial data. The ideal candidate will have a degree in Life Sciences, project management expertise, and experience in regulatory affairs. Responsibilities include managing disclosure requirements, mentoring colleagues, and leading initiatives to optimize processes. This role offers the opportunity to make a significant impact on healthcare access worldwide.