Associate Clinical Trial Manager (PhD) - Cardiovascular

Medpace; Madrid; Presencial; EUR 40.000 - 60.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible work environment

Competitive compensation and benefits package

Structured career paths for professional growth

Employee health and wellness initiatives

Descripción de la vacante

Medpace is seeking an Associate Clinical Trial Manager for their Madrid team. Ideal candidates will have a PhD in Life Sciences and be fluent in English. Responsibilities include managing study activities and maintaining project timelines. This full-time role offers a competitive compensation package and opportunities for professional growth in a flexible work environment, making it a fantastic opportunity for recent graduates aiming to develop their career in clinical trial management.

Formación

• Fluency in English with solid presentation skills.
• Ability to work in a fast-paced dynamic industry within an international team.
• Prior experience within the CRO or pharmaceutical industry is advantageous.

Responsabilidades

• Communicate and collaborate on global study activities.
• Ensure timely delivery of recurrent tasks with high accuracy.
• Compile and maintain project-specific status reports.
• Interact with the internal project team and third-party vendors.
• Provide oversight of the regulatory filing system.

Conocimientos

Analytical skills

Presentation skills

Collaboration

Attention to detail

Educación

PhD in Life Sciences

Descripción del empleo

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.

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

• 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

• PhD in Life Sciences
• Fluency in English with solid 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

• 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