Regulatory Study Start-Up Project Manager - 100% Home based
Fortrea(1 month ago)
About this role
A Regulatory Study Start-Up Project Manager at Fortrea is responsible for coordinating and managing regulatory submissions and approvals for clinical trials in ROI, ensuring compliance with local regulations and timely study initiation. The role involves liaising with regulatory authorities and internal teams to facilitate efficient study start-up processes.
Required Skills
- Regulatory Submissions
- Clinical Trials
- IRBs/IECs
- Regulatory Knowledge
- Project Management
- Compliance
- Localization
- Stakeholder Management
- Documentation
- Process Improvement
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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