Director, Regional Head Site Mgmt & Oversight, Europe - (remote)

CSL SEQIRUS

Europe
Strategic leadership for clinical site operations
Effective conduct and supervision of site management
Alignment with international regulatory standards
The Director, Regional Head Site Management & Oversight provides strategic leadership for clinical site operations, ensuring the effective conduct and supervision of site management activities and oversight for clinical programs within the assigned region

Job Summary

  • The Director, Regional Head Site Management & Oversight provides strategic leadership for clinical site operations, ensuring the effective conduct and supervision of site management activities and oversight for clinical programs within the assigned region.
  • This role will require travel to Investigator Meetings, Investigator sites and CROs.
  • CSL Behring is a global biotherapeutics leader driven by our promise to save lives.

Matching Summary

The Director, Regional Head Site Management & Oversight provides strategic leadership for clinical site operations, ensuring the effective conduct and supervision of site management activities and oversight for clinical programs within the assigned region.

Skills & Requirements

Must-have

  • Strategic leadership for clinical site operations
  • Effective conduct and supervision of site management
  • Alignment with international regulatory standards
  • High-quality execution of clinical programs
  • Lead permanent and functional service-provider teams
  • Cultivate strategic partnerships with service providers and CROs
  • Develop relationships within Medical Affairs and with HCPs

Nice-to-have

  • Advocate for process simplification and burden reduction
  • Represent the voice of the site
  • Improve study materials and operational processes
  • Cultivate strong strategic partnerships

Key Requirements

  • Bachelor’s degree or equivalent in life science, nursing, pharmacy, medical laboratory technology
  • 12 years+ relevant clinical research experience
  • Experience in leading and managing a professional team
  • Strong experience in site management, monitoring and overseeing large/complex global trials
  • Solid understanding of the drug development process
  • Robust budget forecasting and management experience
  • Thorough knowledge of ICH guidelines/GCP
  • Proven experience in overseeing vendors and CROs
  • Experience as a mentor and coach
  • Skilled at independently navigating new indications/approaches
  • Excellent understanding of all tasks involved in a clinical development program

Work Rights

Not specified

Tailored Resume

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