Clinical Project Coordinator for Life Sciences
hace 3 días
Job Summary
Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Clinical Trial Manager to join our Clinical Trial Management team. The successful candidate will be responsible for managing clinical trial activities, collaborating with project coordinators and clinical trial managers, and ensuring timely delivery of tasks with high accuracy.
Key Responsibilities
- Communicate and collaborate on global study activities, working closely with the project coordinator and clinical trial manager
- Compile and maintain project-specific status reports within the clinical trial management system
- Interact with the internal project team, Sponsor, study sites, and third-party vendors
- Manage and perform quality control of our internal regulatory filing system
- Provide oversight and management of study supplies
- Create and maintain project timelines
- Coordinate project meetings and produce quality minutes
Qualifications
- 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 within the CRO or pharmaceutical industry not required but will be advantageous
Benefits
- A competitive salary: $70,000 - $90,000 per year
- An opportunity to work in a fast-paced and dynamic industry
- Collaborative and international team environment
- The chance to develop your career in clinical trial management
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.
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