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Job Description
The CTA is an administrative support role for clinical trials. The role responsibilities include but not limited to the following activities:
Basically:
Safety reports distribution and tracking.
TMF support for country level document uploading to eTMF, assist with eTMF reconciliation, CDA collection, etc.
Support HGRAC site filing documents collection and archiving.
Coordinate with vendor for office supply purchasing, trial related documents printing and translation activity.
Responsible for ABAC (Anti-Bribery and (Anti-)Corruption) check
On site support for investigator meeting.
Support CRM for tracker maintenance and run report from various systems and other activities based on CRM’s requirement.
Contribute to CTA team knowledge by acting as mentor and/or sharing best practices, leading initiatives as required.
Using IT technology to develop tool or work out solution to increase work efficiency and improve work accuracy will be preferred.
For the senior position:
Take initiatives or POC and have leadership to support CTA managers or SMEs on process management or internal and external stakeholder management.
Current Contingent Workers apply
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