Specialist I, Patient Safety Solutions
Fortrea(1 month ago)
About this role
A Clinical Safety specialist responsible for managing the receipt, processing, and reporting of adverse event data from clinical trials and post-marketing sources. The role ensures timely submission to clients and regulatory agencies, maintains safety databases and documentation, and supports pharmacovigilance activities such as signal detection, audits, and project reporting.
Required Skills
- Pharmacovigilance
- Adverse Event Processing
- Data Entry
- MedDRA Coding
- Narrative Writing
- Regulatory Reporting
- Database Reconciliation
- Signal Detection
- SOP Compliance
- Oracle Argus
+5 more
Qualifications
- Associate Degree
- BS/BA
- MS/MA
- PharmD
- Degree in Biological Sciences, Pharmacy, Nursing, Medical Sciences, or Life Sciences (preferred)
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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