Clinical Safety Specialist Jobs in Illinois

Interface with study manager, Clinical Research Organizations, Clinical Research Associates, Data Management, and Pharmacovigilance to assure query resolution.

Work closely with study-specific contacts such as; Clinical Safety Manager, clinical research organization, clinical research associates, data management, and pharmacovigilance.

Triages incoming SAE information in order to fulfill timely reporting according to the authority/regulatory requirements.

Participate in safety surveillance activities for assigned products; and also in area projects/goals. Identify and escalate problems to manager.

2 years clinical experience is required.

Able to apply clinical knowledge to adverse event data collection and assessment.