|Reference # :||20-05350||Title :||Drug Safety Scientist|
|Location :||Lake Zurich, IL|
|Experience Level :||Start Date / End Date :||05/18/2020 / 08/17/2021|
Job Title- Drug Safety Scientist
Location- Lake Zurich, IL
Duration- 3 Months (Possible Extension)
Responsible for Adverse Event processing and other responsibilities as requested per management: ARISg data entry, gCMW data entry and processing; literature review and case processing; Vigilance phone responsibility with core hours (0830 till 1700) . Ability to talk with consumers / patients / health professionals / additional stakeholders in a courteous, cheerful, and cooperative demeanor at all times. Maintains current knowkedge of applicable local and global regulations as they apply to the collection, documentation, and dissemination of adverse drug event information. Attention to detail in reviewing, assessing, and processing of adverse events. Ability to gather data from multiple sources and references to formulate a medically appropriate case narrative, ability to follow-up with consumers / patients/ health propfessionals/ additional stakeholders within company guidelines.
Specific Skills and/or knowledge, credentials, or professional certifications:
R.N. Ability to prioritize and multi-task with minimal supervision. Excellent written and verbal communication skills. Concise, accurate, timely, and appropriate documentation is integral. Utilization of critical thinking skills. Knowledge of ARISg database a plus.