Clinical Trial Manager

hace 1 día


Zaragoza, Zaragoza, España Pharmiweb A tiempo completo
Associate Clinical Trial Manager

Medpace is seeking a highly motivated and detail-oriented Associate Clinical Trial Manager to join our Clinical Trial Management team. As a key member of our team, you will work closely with Project Coordinators and Clinical Trial Managers to ensure the successful execution of clinical trials.

Key Responsibilities:
  • Communicate and collaborate with global study teams to ensure timely delivery of tasks and high-quality results.
  • Compile and maintain project-specific status reports within our clinical trial management system.
  • Interact with internal project teams, sponsors, study sites, and third-party vendors to ensure seamless project execution.
  • Provide oversight and quality control of our internal regulatory filing system and study supplies.
  • Create and maintain project timelines, coordinate project meetings, and produce quality minutes.
Requirements:
  • PhD in Life Sciences with fluency in English and strong presentation skills.
  • Ability to work in a fast-paced dynamic industry within an international team.
  • Prior experience in the CRO or pharmaceutical industry is advantageous but not required.

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, we employ over 5,000 people across 40+ countries. Join us in making a difference in the lives of patients and families affected by disease.



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