Senior Medical Regulatory Writer

Sanofi UK

Bogota, Colombia
Hybrid
High-quality medical documents
Ich and gcp/gvp standards
Therapeutic area expertise
As Senior Medical Regulatory Writer within our Global Medical Services Team, you’ll be responsible for delivering high‑quality medical documents on time and in compliance with internal and external standards and guidelines

Job Summary

  • As Senior Medical Regulatory Writer within our Global Medical Services Team, you’ll be responsible for delivering high‑quality medical documents on time and in compliance with internal and external standards and guidelines.
  • Build strong relationships with medical and pharmacovigilance stakeholders and mentor junior writers by sharing knowledge and expertise.
  • Colombia is one of Sanofi’s key locations for new talents, having a big footprint with the Bogota HUB and its best-in-class operation.

Matching Summary

As Senior Medical Regulatory Writer within our Global Medical Services Team, you’ll be responsible for delivering high‑quality medical documents on time and in compliance with internal and external standards and guidelines.

Skills & Requirements

Must-have

  • high-quality medical documents
  • ICH and GCP/GVP standards
  • Therapeutic Area expertise
  • scientific data interpretation
  • medical literature screening

Nice-to-have

  • stakeholder management
  • ability to work independently
  • mentoring junior writers
  • cross-cultural team collaboration

Key Requirements

  • Previous experience in regulatory writing
  • Degree in life sciences
  • Advanced English level

Work Rights

Not specified

Tailored Resume

Cover Letter