TMF Specialist
IQVIA · Liaoning, China
Clinical OperationsFull-timeCompany career page
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Role summary
Manages trial master file administration and records operations for clinical research projects, including data maintenance, document retrieval, scanning coordination, and compliance monitoring. Requires 3–4 years of clinical research experience, knowledge of GCP and ICH guidelines, strong organizational skills, and proficiency in records management systems.
Privacy & handoff
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