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 division, responsible for leading complex global clinical studies while ensuring operational excellence and strategic delivery. The position is hybrid, requiring work in both Oss and Amsterdam, with a focus on candidates experienced in clinical operations, particularly in oncology and haematology. **

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.
  • 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 offer a dynamic, innovative, international working environment, where you can be part of the development of new medicines that can make a difference to patients' lives.

Matching Summary

Match Score: 75

** Acerta Pharma is seeking a Global Study Director for its Haematology division, responsible for leading complex global clinical studies while ensuring operational excellence and strategic delivery. The position is hybrid, requiring work in both Oss and Amsterdam, with a focus on candidates experienced in clinical operations, particularly in oncology and haematology. **

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 ambition
  • Mentorship and guidance
  • Talent development and career growth
  • Collaborative and ambitious environment

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
  • Proven ability to lead cross functional global teams
  • Strategic thinking capability
  • Excellent senior level communication skills in English

Work Rights

Not specified

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