Offer summary
Qualifications:
High School diploma or equivalent, Fluent in English (speaking, reading, writing), Good communication and interpersonal skills, Ability to embrace new technologies, Minimal travel up to 25% may be required.
Key responsabilities:
- Ensure compliance with clinical operations policies
- Assist with site management activities as sponsor representative
- Maintain and create Trial Master File and project files
- Input clinical tracking information into databases
- Coordinate the ordering and tracking of site supplies