Associate Clinical Trial Manager (PhD) - Cardiovascular

Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Madrid Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

Lea el resumen de esta oportunidad para comprender qué habilidades, incluidas las habilidades interpersonales relevantes y el dominio de paquetes de software, se requieren.

A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities

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• 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
  

Qualifications

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• PhD in Life Sciences
  
• Fluency in English with solid xghoner presentation skills
  
• Ability to work in a fast-paced dynamic industry within an international team
  
• Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
  

Benefits

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• 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
  

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