Safety and Pharmacovigilance Specialist
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POST DATE 8/31/2016
END DATE 10/23/2016
Technical Resources International Inc.
JOB DESCRIPTIONProcess/evaluate serious adverse event reports for developmental & marketed compounds; Prep case safety reports for review & submission to reg auth; Perform med qual ctrl of processed IND Safety Reports, MedWatch Reports & SAE reports; Review protocols & safety info from IND/non-IND studies; Review IND reports prior to reg submission; Prep & conduct training on expedited adverse event reporting & rel processes to clinical sites, trial networks & clients/affiliates; Review MedDRA coding, participate in coding conventions & contribute to MedDRA term selection guidelines.