Senior Medical Regulatory Writer

Sanofi

Bogota, Colombia
Hybrid
High-quality medical documents
Ich and gcp/gvp standards
Therapeutic area expertise
Deliver high-quality medical and regulatory documents on time and in full compliance with all standards and timelines

Job Summary

  • Deliver high-quality medical and regulatory documents on time and in full compliance with all standards and timelines.
  • Build strong relationships with medical and pharmacovigilance stakeholders and mentor junior writers by sharing knowledge and expertise.
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

Matching Summary

Deliver high-quality medical and regulatory documents on time and in full compliance with all standards and timelines.

Skills & Requirements

Must-have

  • high-quality medical documents
  • ICH and GCP/GVP standards
  • Therapeutic Area expertise
  • scientific and regulatory accuracy
  • collaboration with global partners

Nice-to-have

  • stakeholder management
  • ability to work independently
  • mentoring junior writers
  • process excellence
  • audit/inspection readiness

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter