Cardiovascular PhD: Associate Clinical Trial Manager

Medpace

Vlaams-Brabant

Sur place

EUR 55 000 - 85 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Résumé du poste

A leading clinical research organization is seeking an Associate Clinical Trial Manager in Leuven, Belgium. This full-time role requires a PhD in Life Sciences and offers intensive training for recent graduates looking to develop their careers in clinical trial management. Responsibilities include collaboration on global study activities, maintaining project-specific reports, and managing study supplies. The company offers a flexible work environment, competitive compensation, and structured career growth paths.

Qualifications

  • PhD in Life Sciences required for the position.
  • Fluency in English with solid presentation skills is needed.
  • Experience in the CRO or pharmaceutical industry is advantageous but not required.

Responsabilités

  • Communicate and collaborate on global study activities.
  • Ensure timely and accurate delivery of tasks.
  • Compile and maintain project-specific status reports.
  • Interact with internal project team and study sites.
  • Provide oversight and quality control of regulatory filing system.
  • Manage study supplies and coordinate project meetings.

Connaissances

Fluency in English
Solid presentation skills
Ability to work in a fast-paced dynamic industry

Formation

PhD in Life Sciences

Description du poste

A leading clinical research organization is seeking an Associate Clinical Trial Manager in Leuven, Belgium. This full-time role requires a PhD in Life Sciences and offers intensive training for recent graduates looking to develop their careers in clinical trial management. Responsibilities include collaboration on global study activities, maintaining project-specific reports, and managing study supplies. The company offers a flexible work environment, competitive compensation, and structured career growth paths.
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