Senior Associate, Pharmacovigilance - Japan - Remote
Worldwide Clinical Trials(10 days ago)
About this role
Worldwide Clinical Trials is seeking a seasoned Pharmacovigilance professional to join their global team. The role involves reviewing safety data, preparing regulatory safety reports, and ensuring drug safety compliance throughout the clinical trial process.
Required Skills
- SAE Data Review
- Regulatory Reporting
- Clinical Safety
- Database Management
- Pharmacovigilance
- Public Health
- Drug Safety
- Data Analysis
- Communication Skills
- Regulations
About Worldwide Clinical Trials
worldwide.comWorldwide Clinical Trials is a top-rated, full-service global CRO. We provide 30+ years of clinical expertise to benefit your study. Learn more about us here.
View more jobs at Worldwide Clinical Trials →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 Worldwide Clinical Trials
Grants Payments Data Analyst - Europe - Remote
Worldwide Clinical Trials(4 days ago)
Sales Development Account Manager - EU - Remote
Worldwide Clinical Trials(10 days ago)
Senior Clinical Data Manager - UK - Remote
Worldwide Clinical Trials(18 days ago)
Senior/Clinical Payments Specialist - Europe- Remote
Worldwide Clinical Trials(18 days ago)
Similar Jobs
Senior Manager Pharmacovigilance
Clinical Careers Page(27 days ago)
Pharmacovigilance Scientist
Sanofi(12 days ago)
Pharmacovigilance Associate
Clinical Careers Page(5 days ago)
Associate Director, Pharmacovigilance Operations
Relay Therapeutics(18 days ago)
Senior Pharmacovigilance Associate
Clinical Careers Page(17 days ago)
Pharmacovigilance Supervisor
Clinical Careers Page(11 days ago)