Medical Writer

Alvotech

Not specified
Scientific and regulatory documentation
Clinical development through registration
Translate complex scientific data
Alvotech is seeking an experienced Medical Writer to support scientific and regulatory documentation throughout the product lifecycle. The ideal candidate will have a strong background in medical writing, particularly within the biopharmaceutical sector, and possess excellent communication skills to translate complex data into clear documentation

Job Summary

  • The Medical Writer is responsible for overseeing all medical writing activities throughout the product lifecycle, spanning from clinical development through the post marketing phase of our molecules.
  • The role requires an expert communicator who can translate complex scientific, clinical, and safety data into clear, accurate, and compliant documents for global regulatory authorities, healthcare professionals, and internal stakeholders.
  • Join a fast-growing, international company with a diverse and inclusive culture, offering career development, cultural exchange opportunities, and a collaborative environment.

Matching Summary

Match Score: 85

Alvotech is seeking an experienced Medical Writer to support scientific and regulatory documentation throughout the product lifecycle. The ideal candidate will have a strong background in medical writing, particularly within the biopharmaceutical sector, and possess excellent communication skills to translate complex data into clear documentation.

Skills & Requirements

Must-have

  • scientific and regulatory documentation
  • clinical development through registration
  • translate complex scientific data
  • global regulatory authorities
  • cross-functionally with colleagues
  • document management system experience

Nice-to-have

  • excellent scientific storytelling
  • high attention to detail
  • working on biosimilar trials
  • cultural exchange opportunities
  • positive flexible innovative setting

Key Requirements

  • MSc/PhD in Life Sciences, PharmD, MD
  • at least 5 years of experience
  • Strong knowledge of GCP
  • global PV regulations
  • relevant ICH/regulatory guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter