Full time

【Alexion Japan】Clinical development Associate, R&D

Posted by Alexion Pharmaceuticals • June 08, 2026

📍 Japan, Tokyo, Japan

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Description

Position Summary
 The Clinical Development Associate (CDA) contributes to Study Delivery with appropriate quality by having primary responsibility for essential document management and coordinate tasks that improve team performance from a wider perspective during the study process.
Principal Responsibilities
Trial Master File (TMF) Management
 Initiate and lead the set up of TMF including tracking of documents.
Implement of appropriate quality check of the study-related documents in TMF and check GCP and SOP compliance.
Check the status of document storage (Completeness, Timeliness) and share the information to study team.
Coordination of Clinical Trial Notification (CTN)
Set a schedule of necessary actions for CTN submission
Coordinate information collection for CTN and draft it and manage timing of CTN update for regulatory compliance.
JNDA/Inspection
Prepare index/documents required sub...
            

Job Details

Location Japan, Tokyo
Job Type Full time
Category Life Scientists
Posted June 08, 2026
Deadline July 18, 2026

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