Global Study Start-Up Strategy Lead

Jazz Pharmaceuticals

United States

Remote

USD 165,000 - 247,000

Full time

14 days+

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Job summary

Jazz Pharmaceuticals is seeking an Associate Director of Study Start Up Strategy to oversee global start-up planning, manage CRO oversight, and apply data-driven insights to optimize country and site activations. The role requires deep regulatory knowledge, cross-functional leadership, and experience with SSU platforms like CTMS and Veeva Vault.

The role emphasizes strategic guidance, risk mitigation, and continuous process improvement to support rapid and scalable trial activation across

Qualifications

  • Subject matter expert in clinical site start-up with regulatory knowledge.
  • Experience leading global start-up strategy across in-house or outsourced models.
  • Experience leveraging digital technologies to inform study planning and start-up optimization.

Responsibilities

  • Lead or oversee development and execution of SSU start-up strategies and country/site activation plans.
  • Develop site activation projections and input into timelines using data-driven assessment.
  • Provide strategic guidance to internal teams and partners on SSU pathways and CRO oversight.
  • Collaborate cross-functionally to align country/site activation with protocol requirements.

Skills

Clinical site start-up
Cross-functional leadership
Data-driven insights
Leadership
CTMS proficiency
Veeva Vault
Audit readiness
Travel flexibility

Education

Bachelor’s degree in life sciences
Advanced degree preferred

Tools

CTMS
Veeva Vault
Document management systems

Job description

Jazz Pharmaceuticals is seeking an Associate Director of Study Start Up Strategy to oversee global start-up planning, manage CRO oversight, and apply data-driven insights to optimize country and site activations. The role requires deep regulatory knowledge, cross-functional leadership, and experience with SSU platforms like CTMS and Veeva Vault.

The role emphasizes strategic guidance, risk mitigation, and continuous process improvement to support rapid and scalable trial activation across

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