About this role
This role involves leading early phase clinical research projects in China, focusing on innovative drug development and regulatory submission. The individual will work closely with cross-functional teams to design studies, interact with stakeholders, and support clinical and regulatory processes.
Required Skills
- clinical Research
- GCP
- Regulatory Affairs
- Clinical Trial Design
- Medical Monitoring
- Protocol Writing
- Data Analysis
- Investigation Procedures
- Leadership
- Teamwork
About MSD
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