CTA
Ref #: 33469
Employment type: Permanent – Full-Time
Location: Ukraine Kiev
Posted: 03-Nov-2021
Description
Ensure knowledge of relevant local law and regulations.
Support to CT function in submission to Regulatory Authorities
Track and identify IRB/IEC requirements
Support CRA about IRB/IEC submission and others 70%
Ensure that translation of CTA documents is finished within the agreed timeline
Adapt HQ generated documents to local IRB/IEC requirements
Prepare IRB/IEC related trial and site documents and provide to CRA for review
Maintain trial supplies stock at office/ local depot
Ensure that prepare CRF is send to data management within the agreed timeline
Complete minutes of project meeting and other relevant meeting, if required.
Setting up and maintain department database including client details, external
Requirement, suppliers, critical documents and reporting status to head
Quarterly, internal department and regulatory authorities.
Setting up and maintaining document filling systems.
Uploading relevant documents to electronic internal system
Assisting with clinical trial logistics including customs clearance of trial supplies, including lab kits
Shipments monthly trial supplies stock reports drug destruction and collection
Of documentation required for reports.
Handling external and internal relevant stakeholders requires communication made via telephone, e-mail
or face to face
DOCS is an equal opportunity employer – Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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