Safety Science Coordinator I
Fortrea(3 days ago)
About this role
This role involves supporting clinical safety operations related to adverse event processing and regulatory reporting within the pharmaceutical or biotech industry. It includes data entry, report writing, and assisting in maintaining safety databases, ensuring compliance with regulatory standards and company procedures.
Required Skills
- MedDRA
- Data Entry
- Safety Reporting
- Regulatory Compliance
- Clinical Data Management
- Pharmacovigilance
- Database Management
- Medical Writing
- Quality Assurance
- Microsoft Office
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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