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cheryl g

drug safety Associate

Occupation:

Clinical Research

Location:

Middletown, DE

Education Level:

Master

Will Relocate:

YES

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Management and processing of expedited adverse event reports to include the entry of safety data into adverse database and tracking systems, review of adverse events for completeness, accuracy and appropriateness for expedited reporting, generation of queries directly with sites for follow-up information reporting of expedited adverse events. Assessed and triage all incoming cases and process accordingly

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