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Irfa******
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United States
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Last Update: 22.08.2019 at 12:00
Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Greater Philadelphia Area
Country
United States
Description
Overview
This candidate is responsible for the medical content and assessment of post-marketing and/or clinical trial adverse event reports, and serving as a medical resource for the department, and other cross-functional teams as needed.
This position ensures that consistent, timely, and focused medical review for safety cases is conducted according to regulatory and departmental timelines at the individual level and facilitates timely discussion and communication of information related to safety signal evaluation.