Clinical Trial Regulatory Affairs Expert (fixed Term)

Roche UK

Base: 2,700 eur grosspmnthly; bonus: roche annual ...
Hybrid
Clinical trial regulatory activities experience
Eea and row country submission management
Cross-functional team coordination skills
The candidate will serve as a strategic architect for the Clinical Trial Application process across the EEA and ROW after a mentorship period

Job Summary

  • The candidate will serve as a strategic architect for the Clinical Trial Application process across the EEA and ROW after a mentorship period.
  • Roche offers extensive development opportunities including free language courses, international assignments, and a hybrid work model.
  • This role requires managing core CTAs, coordinating with internal departments, and advising program managers on country-specific regulatory changes.

Matching Summary

The candidate will serve as a strategic architect for the Clinical Trial Application process across the EEA and ROW after a mentorship period.

Salary

Base: 2700 EUR gross/monthly; Bonus: Roche Annual Bonus mentioned; Benefits: Monthly transportation allowance, health insurance, home office equipment

Skills & Requirements

Must-have

  • Clinical trial regulatory activities experience
  • EEA and ROW country submission management
  • Cross-functional team coordination skills

Nice-to-have

  • Knowledge of Veeva RIM and CTIS systems
  • Experience with SMT/RAFT meetings
  • Fluent written and spoken English

Key Requirements

  • At least 1 year experience in clinical trial activities
  • BS/BA degree or minimum 3 years relevant pharmaceutical industry experience

Work Rights

Not specified

Tailored Resume

Cover Letter