FSP CTC(Shanghai)
Fortrea(14 days ago)
About this role
This role involves managing site start-up activities and regulatory submissions for clinical trials, ensuring compliance with international standards and local regulations. The person will serve as a primary liaison with investigative sites and regulatory authorities across various countries, contributing to the efficient start-up and maintenance of clinical studies.
Required Skills
- Regulatory Affairs
- Clinical Research
- IRB
- GCP
- Study Start-up
- Documentation
- Regulatory Submissions
- Site Management
- Informed Consent
- CTIS
About Fortrea
fortrea.comFortrea, a leading CRO, advancing clinical trials through patient-focused clinical solutions that accelerate clinical development, drive trial success, and bring innovative therapies to those who need them most.
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