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

CSL Behring

EMEA
Remote
Strategic leadership for clinical site operations
Ensure adherence to international regulatory standards
Lead site management teams
CSL Behring is seeking a Director, Regional Head Site Management & Oversight for the EMEA region, responsible for leading clinical site operations and ensuring compliance with international regulations. The role involves managing site relationships, supporting study delivery, and improving operational processes, requiring significant experience in clinical research and team management

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.
  • The role ensures high-quality execution of clinical programs, acting as the strategic link between therapeutic areas and investigator sites.
  • This role will require travel to Investigator Meetings, Investigator sites and CROs. Anticipated travel >50%.

Matching Summary

Match Score: 85

CSL Behring is seeking a Director, Regional Head Site Management & Oversight for the EMEA region, responsible for leading clinical site operations and ensuring compliance with international regulations. The role involves managing site relationships, supporting study delivery, and improving operational processes, requiring significant experience in clinical research and team management.

Skills & Requirements

Must-have

  • Strategic leadership for clinical site operations
  • Ensure 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
  • Operational oversight of site health and monitoring
  • Proactively mitigate site-level risks

Nice-to-have

  • Advocate for process simplification
  • Represent the voice of the site
  • Navigate new or novel indications

Key Requirements

  • 12+ years relevant clinical research experience
  • Experience leading and managing professional teams
  • Strong experience in site management and monitoring
  • 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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