Position Overview
Responsibilities - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
- Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
- 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;
- Provide oversight and quality control of our internal regulatory filing system;
- Provide oversight and management of study supplies;
- Create and maintain project timelines; and
- Coordinate project meetings and produce quality minutes.
Qualifications - PhD in Life Sciences;
- Research experience must be related to Renal;
- Fluency in English with solid presentation skills;
- Ability to work in a fast-paced dynamic industry within an internati...