Regulatory Submissions Ass Manager II
Fortrea(7 days ago)
About this role
This role involves overseeing regulatory submissions and compliance activities related to clinical trial site readiness, including liaising with regulatory authorities and ethics committees. It requires collaboration across teams to ensure timely and compliant delivery of project milestones in the pharmaceutical or CRO industry.
Required Skills
- Regulatory Submissions
- CTIS
- Clinical Trials
- Regulatory Compliance
- Project Management
- Quality Assurance
- Risk Management
- SOP Development
- Regulatory Affairs
- Drug Development
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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