PhD-Driven CTM: Fast-Track to Trial Leadership

Medpace, Inc.

Heverlee

Sur place

EUR 65 000 - 90 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Competitive compensation programs
Health, retirement, PTO benefits
Occasional WFH after training
Company-sponsored social events

Résumé du poste

Medpace, Inc. is seeking candidates with Radiopharmaceutical or Nuclear Medicine PhDs or post-doctoral research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM).

You will work with Project Coordinators and Clinical Trial Managers on clinical trial management activities, applying analytical and academic skills to administration and management. This role offers an entry path for recent PhD graduates to enter the industry, with comprehensive training, in an

Qualifications

  • PhD in Life Sciences required.
  • Fluency in English with solid presentation skills.
  • Ability to work in a fast-paced dynamic industry within an international team.
  • Prior CRO/pharma industry experience is advantageous but not required.

Responsabilités

  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
  • Compile and maintain project-specific status reports within the clinical trial management system
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors
  • Provide oversight and quality control of our internal regulatory filing system
  • Provide oversight and management of study supplies
  • Create and maintain project timelines
  • Coordinate project meetings and produce quality minutes

Connaissances

English fluency
Presentation skills
Team collaboration
CRO/pharma experience advantageous

Formation

PhD in Life Sciences

Description du poste

Medpace, Inc. is seeking candidates with Radiopharmaceutical or Nuclear Medicine PhDs or post-doctoral research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM).

You will work with Project Coordinators and Clinical Trial Managers on clinical trial management activities, applying analytical and academic skills to administration and management. This role offers an entry path for recent PhD graduates to enter the industry, with comprehensive training, in an

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