Global Study Director – Haematology

Acerta Pharma

Oss, Netherlands
**
Global clinical study leadership
Operational excellence in clinical trials
Ich-gcp and regulatory standards
** Acerta Pharma is seeking a Global Study Director for its Haematology department, responsible for leading complex global clinical studies from operational planning to delivery. The ideal candidate should have extensive experience in clinical operations, particularly in oncology, and strong leadership skills to drive strategic initiatives within a hybrid working environment. **

Job Summary

  • The Global Study Director is a business critical leadership role within our global Haematology organisation, driving operational excellence while thinking strategically at program level.
  • As a GSD you will lead high-priority, complex global clinical studies and play a pivotal role in shaping study delivery strategy, ensuring operational excellence, and demonstrating strong leadership within a highly collaborative and ambitious environment.
  • We highly invest in talent development to drive performance and build meaningful, long-term careers.

Matching Summary

Match Score: 75

** Acerta Pharma is seeking a Global Study Director for its Haematology department, responsible for leading complex global clinical studies from operational planning to delivery. The ideal candidate should have extensive experience in clinical operations, particularly in oncology, and strong leadership skills to drive strategic initiatives within a hybrid working environment. **

Skills & Requirements

Must-have

  • Global clinical study leadership
  • Operational excellence in clinical trials
  • ICH-GCP and regulatory standards
  • Cross-functional global team leadership
  • Oncology experience required

Nice-to-have

  • Strategic thinking and program level
  • Mentorship and guidance
  • Collaborative and ambitious environment
  • Talent development focus

Key Requirements

  • Extensive experience in clinical operations
  • Strong experience leading global clinical studies
  • Deep understanding of drug development
  • Strong knowledge of ICH-GCP
  • Experience managing CRO oversight

Work Rights

Not specified

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