Global Study Manager, Oncology R&d, Early Oncology Clinical

medizinstellenmarkt.de

Study document development
Vendor management
Data delivery enablement
You will turn complex protocols into operational reality, enabling decisive progress in first-in-human and proof-of-concept trials that put patients first

Job Summary

  • You will turn complex protocols into operational reality, enabling decisive progress in first-in-human and proof-of-concept trials that put patients first.
  • Your work will ensure study start-up, recruitment, data delivery and inspection readiness happen without delays.
  • Join us in our unique and ambitious world to transform outcomes for people living with cancer.

Matching Summary

You will turn complex protocols into operational reality, enabling decisive progress in first-in-human and proof-of-concept trials that put patients first.

Skills & Requirements

Must-have

  • Study document development
  • Vendor management
  • Data delivery enablement

Nice-to-have

  • Cross-functional team leadership
  • Strong analytical skills
  • Clear communication skills

Key Requirements

  • Proven experience in study document development
  • Experience with third-party vendor management
  • Familiarity with ICH-GCP and global regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter