Senior Oncology Regulatory Strategy Leader

IQVIA

Durham (NC)

Sur place

USD 186 000 - 519 000

Plein temps

Il y a 3 jours
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Résumé du poste

IQVIA seeks a senior leader to provide regulatory and biostatistical strategy for drug development and lifecycle management. You will support multi-regional programs, interface with clients, and contribute to policy initiatives and publications.

The role involves leadership in novel trial designs, including digital twins, and collaboration with senior management across the organization. Responsibilities include integrating services into client offerings, supporting FDA/EMA engagements, and

Qualifications

  • Bachelor’s Degree required with 15+ years of clinical research/regulatory experience.
  • Broad management and leadership knowledge to lead multiple job areas.
  • Excellent communication and presentation skills; strong business development experience.

Responsabilités

  • Provide leadership and consultancy on regulatory and biostatistical strategies for drug development.
  • Interface with clients as part of the Therapeutic Science & Strategy Unit to provide strategic advice.
  • Support regulatory submissions and engagement with authorities (FDA, EMA) across lifecycle.
  • Contribute to policy initiatives, thought leadership, and scientific publications.
  • Develop and maintain relationships with pharmaceutical/biotech companies and key opinion leaders.

Connaissances

Excellent communication skills
Presentation skills
Business development experience
Leadership
Client-facing consulting

Formation

Bachelor's Degree

Description du poste

IQVIA seeks a senior leader to provide regulatory and biostatistical strategy for drug development and lifecycle management. You will support multi-regional programs, interface with clients, and contribute to policy initiatives and publications.

The role involves leadership in novel trial designs, including digital twins, and collaboration with senior management across the organization. Responsibilities include integrating services into client offerings, supporting FDA/EMA engagements, and

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