Global Regulatory Pre-Award Strategy Director

Worldwide Clinical Trials

Barcelona

Presencial

EUR 90.000 - 120.000

Jornada completa

14 días+
Generador de candidaturas

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Descripción de la vacante

Worldwide Clinical Trials in Barcelona is seeking a Director of Regulatory Pre-Award Strategy to establish operational strategies and achieve performance goals in regulatory affairs. This senior leadership role involves managing teams and providing regulatory expertise, ensuring project compliance and timely deliverables.

The ideal candidate will have a strong background in clinical research, extensive experience in the pharmaceutical or CRO industry, and outstanding leadership skills. This position presents a unique opportunity to lead regulatory strategies in a dynamic environment.

Formación

  • Minimum 10 years within pharmaceutical/CRO industry with senior regulatory or clinical start-up experience.
  • Demonstrated ability to independently manage multiple tasks in a fast-paced environment.

Responsabilidades

  • Oversee regulatory affairs activities and manage teams.
  • Provide expert regulatory advice and drive planning for regulatory activities.
  • Foster relationships for timely submission of regulatory dossiers.

Conocimientos

Oral and written communication skills
Leadership and organizational management
Proficiency in MS-Office applications
Understanding of clinical research principles
Interpersonal skills

Educación

Bachelor's degree in medical, biological, physical, health, pharmacy or related science
Nursing degree or equivalent life science degree (plus 8 years clinical research experience)

Herramientas

Microsoft Word
Excel
PowerPoint

Descripción del empleo

Worldwide Clinical Trials in Barcelona is seeking a Director of Regulatory Pre-Award Strategy to establish operational strategies and achieve performance goals in regulatory affairs. This senior leadership role involves managing teams and providing regulatory expertise, ensuring project compliance and timely deliverables.

The ideal candidate will have a strong background in clinical research, extensive experience in the pharmaceutical or CRO industry, and outstanding leadership skills. This position presents a unique opportunity to lead regulatory strategies in a dynamic environment.

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