Descripción del trabajo

Experteer Overview As an Associate Clinical Trial Manager, you will support general clinical trial activities within a cross-functional team. You will translate research skills into practical clinical project administration, working with Project Coordinators and Clinical Trial Managers. The role offers intensive training, international exposure, and a fast-paced path into clinical trial management. You will help drive study execution, quality, and timelines in a purpose-driven, collaborative environment.
Compensaciones / Beneficios

Collaborate on global study activities with the project coordinator and clinical trial manager
Ensure timely delivery of recurring tasks with high accuracy
Compile and maintain project-specific status reports in the clinical trial management system
Interact with internal project teams, Sponsor, study sites, and third-party vendors




Quality control of the internal regulatory filing system
Provide oversight and management of 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 skills
Ability to work in a fast-paced dynamic industry within an international team
CRO or pharmaceutical industry experience is not required but advantageous
Requisitos principales

competitive compensation
comprehensive health, wellness, retirement, and PTO benefits
office-based with occasional WFH for eligible positions
on-site mentoring and defined career paths
industry-renowned onboarding and training programs
ongoing training and learning opportunities

📌 Associate Clinical Trial Manager (Madrid)
🏢 Medpace
📍 Madrid