Global Clinical Program Lead — Senior Medical Director

CSL

King of Prussia (PA)

Hybrid

USD 317,000 - 409,000

Full time

3 days ago
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Job summary

CSL Behring seeks a Senior Medical Director, Global Clinical Program Leader (GCPL) to design and lead the clinical strategy for a medicine, guiding the Clinical Development Team in a matrixed setting. The role reports to the Global Clinical Lead and requires strong scientific leadership and regulatory acumen.

The position is Hybrid, onsite in the posted locations with at least 3 days onsite weekly and relocation not provided.

Qualifications

  • MD/PhD/PharmD in life science/healthcare required; board certification preferred.
  • 5+ years of clinical development experience in pharma with study data review/evaluation.
  • Experience leading in a matrixed environment and stakeholder management.

Responsibilities

  • Provide leadership to the Clinical Development Team (CDT) and ensure representation in cross-functional discussions.
  • Oversee development and maintenance of the Clinical Development Plan (CDP) aligned with PST and TALT.
  • Integrate internal and external expert contributions to strategy and study design.
  • Ensure alignment with CSL Behring processes, GCP and ICH regulations; drive decision making within the CDT.
  • Serve as clinical development representative on cross-functional teams (SET, SMT, BRAT, BET, EAST).
  • Develop and execute Medical Monitoring Plan (MMP) strategy; act as medical monitor for trials.

Skills

Leadership
Stakeholder management
Regulatory knowledge
Medical writing
Data interpretation
Problem solving
Communication
Cross-functional collaboration

Education

MD/PhD/PharmD in life science/healthcare
Board Certification (USA) or equivalent

Job description

CSL Behring seeks a Senior Medical Director, Global Clinical Program Leader (GCPL) to design and lead the clinical strategy for a medicine, guiding the Clinical Development Team in a matrixed setting. The role reports to the Global Clinical Lead and requires strong scientific leadership and regulatory acumen.

The position is Hybrid, onsite in the posted locations with at least 3 days onsite weekly and relocation not provided.

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