Safety Science Coordinator - 1
Fortrea(4 days ago)
About this role
This role involves supporting clinical safety operations by processing adverse event reports and ensuring regulatory compliance. The job includes data entry, report writing, and coordinating safety documentation within a team environment. It offers an opportunity to contribute to pharmacovigilance and clinical safety in the pharmaceutical or biotechnology industry.
Required Skills
- MedDRA
- Safety Data Entry
- Regulatory Submissions
- Clinical Data Management
- Pharmacovigilance
- Data Reconciliation
- Quality Assurance
- Safety Reporting
- Medical Affairs
- Pharmaceutical Industry
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.
View more jobs at Fortrea →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Fortrea
Similar Jobs
Safety & PV Specialist I - Medical Device & PQC
Clinical Careers Page(6 days ago)
Safety & PV Specialist I - Medical Device - Case Processing
Clinical Careers Page(11 days ago)
Ekspert / Ekspertka ds. Bezpieczeństwa Farmakoterapii
Polpharma(11 days ago)
Pharmacovigilance Associate
Clinical Careers Page(5 days ago)
Pharmacovigilance Associate
Clinical Careers Page(17 days ago)
Local Case Intake Advisor
American Association of Physicists in Medicine(2 months ago)