Director, Clinical Operations Lead

CSL Behring

Gb
**
Clinical study operational strategy
End-to-end study management
Vendor selection and oversight
** CSL Behring is seeking a Director of Clinical Operations Lead to oversee the operational strategy and management of complex clinical studies. The role requires extensive experience in clinical research, project management, and team leadership within the pharmaceutical industry, and offers a hybrid work model. **

Job Summary

  • The Director Clinical Operations Lead is accountable for the development of the operational strategy for clinical study(ies) and/or clinical program(s) as well as end-to-end study management and delivery of all operational activities and budget management.
  • Responsibilities encompass support to the development of the operational strategy for our most complex studies and ensuring achievement of all program goals within established timelines, budget, and quality standards.
  • This role must be experienced in working in a matrix environment with cross-functional responsibilities associated with trial execution and overall therapeutic area clinical development planning.

Matching Summary

Match Score: 75

** CSL Behring is seeking a Director of Clinical Operations Lead to oversee the operational strategy and management of complex clinical studies. The role requires extensive experience in clinical research, project management, and team leadership within the pharmaceutical industry, and offers a hybrid work model. **

Skills & Requirements

Must-have

  • clinical study operational strategy
  • end-to-end study management
  • vendor selection and oversight
  • ICH guidelines and GCP compliance
  • cross-functional team leadership

Nice-to-have

  • agile team environment
  • dynamic biotech ecosystems
  • knowledge sharing across therapeutic areas
  • continuous improvement initiatives

Key Requirements

  • Minimum 12 years relevant clinical research experience
  • Bachelor's degree or equivalent in life science or related area
  • Experience leading and managing professional staff
  • Experience overseeing large/complex global clinical trials
  • Robust budget forecasting and management experience

Work Rights

Not specified

Tailored Resume

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