Global Study Director – Haematology

Acerta Pharma

Oss, Netherlands
**
Global clinical study leadership
Operational excellence in clinical trials
Ich-gcp and regulatory compliance
** Acerta Pharma is seeking a Global Study Director in Haematology to lead complex global clinical studies, ensuring operational excellence and strategic delivery. The role requires extensive experience in clinical operations, particularly in oncology, and offers a hybrid working model until the company's relocation to Amsterdam. **

Job Summary

  • The Global Study Director is a business critical leadership role responsible for the end to end operational planning and delivery of complex global clinical studies within a program.
  • This role requires strategic delivery, leadership and ownership, and strong stakeholder management with Senior Global Program Directors, Medical Lead, Regulatory Affairs, Manufacturing, external partners and CROs.
  • AstraZeneca offers a dynamic, innovative, international working environment with opportunities for talent development, good salary and secondary benefits, and a hybrid working model.

Matching Summary

Match Score: 75

** Acerta Pharma is seeking a Global Study Director in Haematology to lead complex global clinical studies, ensuring operational excellence and strategic delivery. The role requires extensive experience in clinical operations, particularly in oncology, and offers a hybrid working model until the company's relocation to Amsterdam. **

Skills & Requirements

Must-have

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

Nice-to-have

  • Strategic thinking and program ambition
  • Mentorship and guidance skills
  • Proactive risk management
  • Collaborative and ambitious environment

Key Requirements

  • Extensive experience in clinical operations
  • Strong experience leading global clinical studies
  • Oncology experience required
  • 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

Work Rights

Not specified

Tailored Resume

Cover Letter