Regulatory Affairs Officer , Iqvia Biotech

IQVIA UK

São Paulo, Brazil
Regulatory team lead experience
Clinical trial regulatory documentation
Engagement with competent authorities
Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing

Job Summary

  • Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing.
  • Engage directly with clients to clarify clinical trial regulatory pathways and address feedback.
  • Provide guidance and feedback to junior colleagues and support training initiatives.

Matching Summary

Serve as Regulatory Team Lead on complex global studies, including oversight of technical writing and submission publishing.

Skills & Requirements

Must-have

  • Regulatory Team Lead experience
  • Clinical trial regulatory documentation
  • Engagement with Competent Authorities

Nice-to-have

  • Problem-solving mindset
  • Fast-paced environment adaptability
  • Training and continuous improvement support

Key Requirements

  • Bachelor’s or Master’s degree in Life Sciences
  • 3–4 years of relevant clinical trial regulatory experience
  • Strong understanding of R&D continuum

Work Rights

Not specified

Tailored Resume

Cover Letter