1.Review, develop, and maintain regulatory documents and safety databases
2.Conduct PV: receiving, processing, submitting, maintaining safety cases/regulatory
data, and medical coding
3.Establish and facilitate communication with study sites, the EC/IRB, and health
authorities
4.As appropriate, assist Bestat and relevant parties in facilitating medical monitoring
and regulatory processes, management, and policies
1.Planning, coordinating, and conducting audits :
Clinical trial audits、Supplier audits、Audit reports
2.Risk and quality management :
Identify and follow up on corrective and preventive actions for quality-related issues
3.Independent activities :
Assisting in the organization and management of independent committees to ensure their operations comply with relevant regulations
Randomization code quality control
4.Training :
Planning and maintaining the training system (training programs, training materials, and certificate management)、Training record analysis
5.Document management :
SOPs, policies, and manuals: developing, maintaining, and updating company、
SOPs, policies, and manuals to ensure they align with the latest regulatory、
requirements and industry standards、Archives: managing the clinical trial-related documents that are archived in the archiving room
6.Other assigned QA tasks