Global Regulatory Projects Lead for GRAPS Enablement

Ascendis Pharma

Gentofte Kommune

On-site

DKK 900,000 - 1,200,000

Full time

5 days ago
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Job summary

Ascendis Pharma is seeking an experienced Associate Project Director to lead the GRAPS Enablement & Insights function within Global Regulatory Affairs & Patient Safety. You will translate priorities into integrated plans and drive execution across Global Regulatory Affairs, Global Patient Safety, and enterprise functions in a highly regulated, global environment.

You will work with the GRAPS Leadership Team and cross-functional stakeholders to strengthen quality, compliance, predictability, and

Qualifications

  • Experience leading cross-functional programs with senior stakeholders across multiple geographies and vendors.
  • Strong command of project and program management disciplines and governance.
  • Knowledge of drug development, regulatory, and pharmacovigilance domains.

Responsibilities

  • Lead GRAPS projects from initiation through closeout with clear scope, milestones, budgets and risk controls.
  • Translate priorities into roadmaps and integrated execution plans across Regulatory Affairs and Patient Safety.
  • Establish governance, dashboards, and decision materials for executive audiences.
  • Coordinate stakeholders across multiple functions and external partners.
  • Drive standardized, scalable processes while ensuring compliance and inspection readiness.

Skills

Cross-functional leadership
Project management
Stakeholder management
GxP/regulatory knowledge
Dashboard reporting

Education

Bachelor’s or Master’s degree in life sciences / business / PM

Tools

Microsoft 365
PM certification (PMP/PRINCE2)

Job description

Ascendis Pharma is seeking an experienced Associate Project Director to lead the GRAPS Enablement & Insights function within Global Regulatory Affairs & Patient Safety. You will translate priorities into integrated plans and drive execution across Global Regulatory Affairs, Global Patient Safety, and enterprise functions in a highly regulated, global environment.

You will work with the GRAPS Leadership Team and cross-functional stakeholders to strengthen quality, compliance, predictability, and

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