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

CSL SEQIRUS

Multiple Locations
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Strategic leadership for clinical site operations
Adherence to international regulatory standards
Lead site management teams
** CSL Seqirus is seeking a Director, Regional Head Site Management & Oversight for their EMEA region, responsible for leading clinical site operations and ensuring compliance with regulatory standards. This remote position requires extensive experience in clinical research and site management, aiming to enhance relationships with investigators and service providers. **

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.
  • Responsible for operational oversight of the site, site health and monitoring activities, and identifying and proactively mitigating site-level risks impacting recruitment, retention, data quality, or compliance.
  • Build and maintain strong, trusted relationships with investigators and site staff, serving as the sponsor primary point of contact for assigned studies.

Matching Summary

Match Score: 75

** CSL Seqirus is seeking a Director, Regional Head Site Management & Oversight for their EMEA region, responsible for leading clinical site operations and ensuring compliance with regulatory standards. This remote position requires extensive experience in clinical research and site management, aiming to enhance relationships with investigators and service providers. **

Skills & Requirements

Must-have

  • strategic leadership for clinical site operations
  • adherence to international regulatory standards
  • lead site management teams
  • cultivate strategic partnerships with service providers and CROs
  • develop relationships within Medical Affairs and with HCPs

Nice-to-have

  • advocate for process simplification
  • represent the voice of the site
  • cultivating strong strategic partnerships

Key Requirements

  • 12+ years relevant clinical research experience
  • Experience leading and managing a professional team
  • Solid understanding of the drug development process
  • Robust budget forecasting and management experience
  • Thorough knowledge of ICH guidelines/GCP
  • Proven experience overseeing vendors and CROs
  • Experience as a mentor and coach

Work Rights

Not specified

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