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

CSL Behring

EMEA
**
Strategic leadership for clinical site operations
Ensuring effective conduct and supervision of site management
Alignment with overall strategy and regulatory standards
** CSL Behring is seeking a Director, Regional Head Site Management & Oversight for their EMEA region, responsible for leading clinical site operations, ensuring compliance, and fostering relationships with investigators and CROs. The role requires significant experience in clinical research, team management, and a solid understanding of the drug development process. **

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 is 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.
  • The position requires building and maintaining strong, trusted relationships with investigators and site staff, serving as the sponsor's primary point of contact for assigned studies, and requires travel to Investigator Meetings, Investigator sites and CROs (anticipated travel >50%).

Matching Summary

Match Score: 75

** CSL Behring is seeking a Director, Regional Head Site Management & Oversight for their EMEA region, responsible for leading clinical site operations, ensuring compliance, and fostering relationships with investigators and CROs. The role requires significant experience in clinical research, team management, and a solid understanding of the drug development process. **

Skills & Requirements

Must-have

  • Strategic leadership for clinical site operations
  • Ensuring effective conduct and supervision of site management
  • Alignment with overall strategy and regulatory standards
  • Cultivating strategic partnerships with service providers and CROs
  • Building and maintaining strong relationships with investigators and site staff

Nice-to-have

  • Advocating for process simplification and burden reduction
  • Representing the voice of the site in cross-functional discussions
  • Developing reporting personnel for complex project management

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
  • 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

Work Rights

Not specified

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