Clinical Trial Manager
hace 3 semanas
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.
Job SummaryWe are seeking a highly motivated and detail-oriented Associate Clinical Trial Manager to join our Clinical Trial Management team. The successful candidate will have a PhD in Life Sciences and/or Post-Doctoral Research experience, with a strong desire to transfer and apply analytical and academic skills in clinical project administration and management.
Key Responsibilities- Communicate and collaborate with global study teams to ensure timely delivery of recurrent tasks with high accuracy
- Compile and maintain project-specific status reports within the clinical trial management system
- Interact with internal project teams, sponsors, study sites, and third-party vendors to provide oversight and quality control
- Create and maintain project timelines, coordinate project meetings, and produce quality minutes
- 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 in the CRO or pharmaceutical industry is not required but will be advantageous
At Medpace, we value our employees and offer a range of benefits, including hybrid work-from-home options, competitive PTO packages, company-sponsored employee appreciation events, and flexible work schedules. We are committed to providing a supportive and inclusive work environment that fosters growth and development.
Join us in our mission to accelerate the global development of safe and effective medical therapeutics.
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