Technical Resources International, Inc.
Manage and process all SAEs as per project specific instructions
Document Control: maintain electronic files for department, perform file case searches, maintain file room for the department and use department databases to track, manage and control issued documents; assign various tracking numbers
Track and process assigned pharmaceutical and Data Management Center (DMC) queries
Assist in the preparation of contract-required reports
Generate specified data reports from the safety database as requested
Process and edit safety narratives for IND and Non-IND Adverse Event (AE) cases as required
Distribute Safety Information according to project specific requirements
Assist in processing of MedDRA coding tasks
Perform QC on AE submissions
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Employee Type Full-Time
Location Bethesda, MD
Job Type Biotech
Experience Not Specified
Date Posted 07/02/2022
Job ID 63/34/555