Senior/Regulatory Affairs Manager- APAC- Remote
Worldwide Clinical Trials(19 days ago)
About this role
Worldwide Clinical Trials is seeking a senior regulatory professional to lead and coordinate regulatory submissions across EMEA, Asia Pacific, and Latin America for clinical trials. The role involves providing expert advice, mentoring staff, and ensuring compliance with international standards to support the development and approval of medical products.
Required Skills
- Regulatory Submissions
- ICH GCP
- Clinical Trials
- Project Management
- Cross-cultural Communication
- Regulatory Strategy
- Documentation Review
- Mentoring
- Biological Sciences
- International 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.
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