Clinical Trial Manager
hace 2 días
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 be responsible for managing clinical trials from start to finish, ensuring timely delivery of tasks and maintaining high accuracy.
Key Responsibilities:
- Communicate and collaborate with global study teams to ensure seamless project execution
- Compile and maintain project-specific status reports within our clinical trial management system
- Provide oversight and quality control of our internal regulatory filing system
- Manage study supplies and coordinate project meetings
- Develop and maintain project timelines and ensure timely delivery of tasks
Requirements:
- PhD in Life Sciences
- Fluency in English with 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 not required but will be advantageous
About Medpace:
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.
Why Medpace?
At Medpace, we value our people, purpose, and passion. We strive to make a difference in the lives of patients and families affected by disease. Join us today and be part of a team that is dedicated to improving human health.
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