FSO SSU(North Cities)
Fortrea(2 months ago)
About this role
A Regulatory Submissions Specialist at Fortrea supports clinical study regulatory activities across assigned countries. The role serves as a primary site contact for collection and management of investigator and regulatory essential documents and aids in preparing submissions to ethics committees and regulatory authorities. It is an entry-level position that develops regulatory knowledge and works under supervision of senior staff.
Required Skills
- Regulatory Submissions
- Document Management
- IRB IEC
- Quality Review
- CTIS
- ICH GCP
- Stakeholder Communication
- Tracking Systems
- Site Liaison
Qualifications
- University Degree (Life Science Preferred)
- Nursing Certification
- Medical Laboratory Certification
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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