Scientific Director

Octapharma AG

Lachen, Switzerland
On-site
Global clinical development strategy
Evidence-generation planning
Cross-functional scientific teams
Octapharma AG is seeking a Scientific Director to lead global clinical development activities from their headquarters in Lachen, Switzerland. The ideal candidate will have a strong background in clinical development, regulatory frameworks, and scientific leadership, contributing to the company's mission of producing life-saving medicines

Job Summary

  • The Scientific Director provides high-level scientific and strategic leadership across global clinical development activities, contributing to long-term portfolio strategy and guiding evidence-generation planning.
  • The role leads cross-functional scientific teams, collaborates with international stakeholders, and ensures strong oversight of external partners and governance bodies.
  • Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines, aiming to make people's lives better.

Matching Summary

Match Score: 85

Octapharma AG is seeking a Scientific Director to lead global clinical development activities from their headquarters in Lachen, Switzerland. The ideal candidate will have a strong background in clinical development, regulatory frameworks, and scientific leadership, contributing to the company's mission of producing life-saving medicines.

Skills & Requirements

Must-have

  • global clinical development strategy
  • evidence-generation planning
  • cross-functional scientific teams
  • regulatory frameworks (ICH, GCP, EMA, FDA)
  • vendor and partner management

Nice-to-have

  • family values and long-term perspective
  • skilled and fun colleagues
  • informal organization
  • diversity and equal opportunities

Key Requirements

  • Advanced degree in Medicine (MD), Pharmacy, Life Sciences or related field
  • Extensive experience in clinical development strategy
  • Proven track record in leading global clinical programs
  • Strong expertise in regulatory frameworks
  • Fluent in English (spoken and written)

Work Rights

Not specified

Tailored Resume

Cover Letter