Posted:1 week ago|
Platform:
On-site
Full Time
Assist in the collection, cleaning, and validation of clinical trial data from various sources.
Perform data entry and data review activities to ensure quality and integrity.
Support database setup, testing, and maintenance activities.
Track and manage queries related to data inconsistencies and work with clinical sites to resolve them.
Maintain documentation in compliance with Good Clinical Practice (GCP) and standard operating procedures (SOPs).
Collaborate with cross-functional teams including clinical operations, biostatistics, and medical writing.
Support the preparation of data management reports and metrics.
Participate in team meetings, training sessions, and project discussions.
CLARIWELLGLOBAL SERVICES LLP
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