Offer summary
Qualifications:
High School diploma or equivalent, Good communication and interpersonal skills, Ability to embrace new technologies, Up to 25% travel may be required.
Key responsabilities:
- Perform activities in compliance with applicable Corporate and Clinical Operations policies
- Assist with site management activities and communicate with sites to ensure compliance
- Maintain Trial Master File (TMF), project files, site manuals
- Coordinate team meetings, manage mailbox, track and ship supplies, maintain databases and update clinical information