Efficiency in conducting literature searches for authoring various types of reports.
Author/review various safety reports for global regulatory submissions for clients, including Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Periodic Benefit-Risk Evaluation Reports, Bridging reports and other clinical documents as assigned.
Master’s/Bachelor’s degree in Pharmacy/related science area.
At least 1 year experience in the pharmaceutical industry
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