Senior/Specialist, Regulatory & Site Activation - Australia - Remote
Worldwide Clinical Trials(1 month ago)
About this role
A Regulatory Affairs professional at a global Contract Research Organization supporting regulatory activities across international clinical studies. The role focuses on preparing and coordinating regulatory submissions, maintaining country-specific patient information and labeling, and ensuring compliance with ICH GCP and local regulatory requirements.
Required Skills
- Regulatory Submissions
- Document Review
- Labeling
- Clinical Research
- Project Management
- Communication
- MS Office
- Multilingual
Qualifications
- Bachelor's Degree in Medical, Biological, Physical, Health, Pharmacy or Related Sciences
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.
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