Fortrea·2 months ago
2 months ago
Site Start-Up Specialist
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About this role
Join Our Team and Drive Clinical Research Success! At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pi...
Skills
- ich/gcp compliance
- regulatory submissions
- site start-up processes
- ra regulations
- irb/iec regulations
- ec/irb/third body/regulatory authority documentation
- patient informed consent forms
- document management systems
- stakeholder management
- mentorship
Company
Fortrea
Maidenhead, United Kingdom
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