Director, Epidemiology

Scorpion Therapeutics

United States

Hybrid

USD 180,000 - 240,000

Full time

9 days ago
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Job summary

CSL Behring seeks a Lead Epidemiology role to drive strategy and execution for designated products, supporting R&D and commercial efforts. The position involves developing research strategies, guiding study design, data collection, analysis, and reporting, with input to regulatory submissions and development plans.

Hybrid work in King of Prussia, PA or Waltham, MA with three onsite days. The focus includes rare conditions, post-marketing safety, and advancing real-world evidence in a

Qualifications

  • Doctoral degree in Epidemiology or related field with 10+ years pharma experience.
  • Extensive experience in epidemiologic research and cross-functional leadership.
  • Proven ability to advise product teams and manage regulatory documentation.

Responsibilities

  • Develop and oversee epidemiology research strategies, study design, data collection, analysis, and reporting.
  • Contribute epidemiologic data to regulatory submissions and development plans.
  • Conduct benefit-risk assessments and advance real-world evidence utilization.
  • Support department development and promote best practices.

Skills

Epidemiology expertise
Cross-functional leadership
Regulatory documentation

Education

PhD in Epidemiology or related field
MS in Epidemiology or related field

Job description

Lead epidemiology activities for CSL Behring’s designated products, supporting R&D and commercial efforts through strategic research planning and execution.

Responsibilities
  • develop and oversee epidemiology research strategies, manage study design, data collection, analysis, and reporting
  • contribute epidemiologic data to regulatory submissions (e.g., safety reports, development plans)
  • conduct benefit-risk assessments and advance real-world evidence (RWE) utilization
  • support department development and promote best practices
Qualifications
  • Doctoral degree in Epidemiology or related field with 10+ years (PhD) or Master's with 12+ years pharma experience
  • extensive experience in epidemiologic research, cross-functional team leadership, and regulatory documentation
  • proven ability to advise product teams and lead organizational initiatives
High-Value
  • focus on rare and serious conditions such as hemophilia and primary immune deficiencies, with emphasis on post-marketing safety, benefit-risk assessment, and RWE
  • hybrid role based in King of Prussia, PA or Waltham, MA with 3 days onsite
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