Director, Site Engagement & Strategy

CSL

Waltham (MA)

Hybrid

USD 130,000 - 170,000

Full time

13 days ago
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Job summary

CSL Plasma Inc. seeks an Associate Director, Site Engagement Lead to design and execute a strategic, cross-functional engagement plan for clinical programs, optimizing site feasibility, recruitment, and experience.

The role partners with Clinical Development, Trial Management, Site Management and Medical Affairs to align site perspectives with study goals, driving measurable improvements across the study lifecycle.

Qualifications

  • Advanced degree in life sciences, pharmacy, medicine, or related field.
  • 10+ years of experience in clinical research, clinical operations, medical affairs, site engagement, or related discipline.
  • Experience across global clinical development; sponsor or CRO environments.

Responsibilities

  • Develop and refine the engagement strategy for assigned programs and studies.
  • Lead a cross-functional engagement team across the study lifecycle.
  • Translate site feedback and external intelligence into actionable insights for feasibility, site selection and recruitment.
  • Identify risks and opportunities; challenge assumptions affecting study feasibility and site experience.
  • Collaborate across functions and geographies to ensure coordinated site engagement.

Skills

Strategic thinking
Influence without authority
Cross-functional collaboration
Analytical thinking
Execution focus
Stakeholder management
Communication
Travel up to 30%

Education

Advanced degree in life sciences/pharmacy/medicine
PhD/PharmD/MD or equivalent preferred

Tools

Power BI
Smartsheet
PowerPoint
Excel

Job description

CSL Plasma Inc. seeks an Associate Director, Site Engagement Lead to design and execute a strategic, cross-functional engagement plan for clinical programs, optimizing site feasibility, recruitment, and experience.

The role partners with Clinical Development, Trial Management, Site Management and Medical Affairs to align site perspectives with study goals, driving measurable improvements across the study lifecycle.

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