Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL SEQIRUS

King of Prussia, PA, USA
Base: $338,000 - $400,000; bonus/equity: incentive...
Hybrid (3 days onsite)
Design and execution of clinical strategy
Medical monitor oversight responsibilities
Gcp and ich regulatory compliance
CSL Seqirus is seeking a Senior Director, Global Clinical Program Lead for Immunoglobulin, who will be responsible for leading clinical development strategies and ensuring compliance with regulatory standards. The position is hybrid and requires significant experience in clinical development, particularly in the pharmaceutical industry

Job Summary

  • The role involves leading the design and execution of clinical strategy to support the development of immunoglobulin medicines.
  • Candidates will serve as a medical monitor or provide oversight to ensure high-quality clinical and scientific standards are met.
  • CSL Behring is a global biotherapeutics leader committed to saving lives through innovative plasma fractionation and recombinant protein technologies.

Matching Summary

Match Score: 85

CSL Seqirus is seeking a Senior Director, Global Clinical Program Lead for Immunoglobulin, who will be responsible for leading clinical development strategies and ensuring compliance with regulatory standards. The position is hybrid and requires significant experience in clinical development, particularly in the pharmaceutical industry.

Salary

Base: $338,000 - $400,000; Bonus/Equity: Incentive compensation and equity included; Benefits: Not specified

Skills & Requirements

Must-have

  • Design and execution of clinical strategy
  • Medical monitor oversight responsibilities
  • GCP and ICH regulatory compliance
  • Cross-functional delivery team leadership
  • Regulatory interaction package preparation

Nice-to-have

  • Agile team collaboration experience
  • Dynamic biotech ecosystem knowledge
  • Strategic decision-making facilitation

Key Requirements

  • MD Board Certified in Pulmonology preferred
  • 5+ years clinical development industry experience
  • Working knowledge of pharmaceutical regulatory processes

Work Rights

Not specified

Tailored Resume

Cover Letter