Clinical Assistant (FSP), Beijing
BEIJING, China 求人ID R0000031876 Category Clinical TrialsAbout this Role
1.Support trial during Conduct
Site communications
- Maintain site contact and relevant vendor and regulatory document tracker (tracking of medical licenses and follow-up/annual collection reminders)
- Printing/mailing documents and equipment to sites (if CRA is not responsible for it)
Vendor communication
- Support CTM to inform TDS about trial events to trigger document collections for critical documents (eg. Investigator Brochures, signature pages)
- Co-ordinating translations of documents after review/translation (approvals, applications, advertising, patient materials, ICFs etc.) and submit for TMF filing
- Support CTM to inform TDS about trial events to trigger document collection
- Support production and create local signature pages for local/global amendments
- Resolving COPI reports ,monthly QC document findings
- Responsible for site address /personnel change, notifications and updates to related forms, supplies and vendor’s spreadsheets etc.
- Ordering trial supplies and sending to sites (if CRO cannot support)
- Maintain Paper Trial Master File if applicable
Requirement:
1. At least 1 year CTA related working experiences;
2. Good communication and English skill
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