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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Job Snapshot

Employee Type Full-Time

Location Bethesda, MD

Job Type Biotech

Experience Not Specified

Date Posted 07/02/2022

Job ID 63/34/555

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