Experteer Overview
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As an Associate Clinical Trial Manager in Madrid, you translate your PhD-level research and analytical skills into clinical project administration. You will collaborate with project coordinators and clinical trial managers to drive global study activities and ensure timely, accurate task delivery. The role offers intensive onboarding, an international environment, and a clear path toward a clinical trial management career in a cutting-edge therapeutic area. You’ll contribute to regulatory oversight, study supply management, and project planning, shaping how trials progress from initiation to execution.
Compensaciones / Ventajas
• Communicate and collaborate on global study activities with project coordinators and clinical trial managers
• Ensure timely delivery of recurrent tasks with high accuracy
• Compile and maintain project-specific status reports in the CTM system
• Interact with internal project team, Sponsor, study sites, and third-party vendors
• Oversee and quality-check the internal regulatory filing system
• Oversee and manage study supplies
• Create and maintain project timelines
• Coordinate project meetings and produce quality minutes
Responsabilidades
• PhD in Life Sciences
• Fluency in English with solid presentation xqbhyrx skills
• Ability to work in a fast-paced dynamic industry within an international team
• Prior CRO or pharmaceutical industry experience not required but advantageous
Requisitos principales
• Competitive compensation
• Comprehensive health and retirement benefits
• PTO and wellness benefits
• WFH flexibility after training
• On-site mentors
• Defined career paths and onboarding/training programs