Clinical Research Associate
Posted on :
12-01-2024
Employer Active
1 Vacancy
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Job Description
Req ID : 806020
Administers cognitive testing per sponsor protocol data analysis; Ensures data collection and administration follows appropriate Federal, State, and University guidelines; Ensures administration and collection of assessments adheres to study protocols.
Coordinates multiple clinical trials studies; Provides and documents informed consent; Works within various systems to record and collect data including electronic databases, patient records, and status logs; Monitors medical record and lab sample collection; Ensures lab sample collection follows infection control and safety procedures.
Employment Type
Full Time
Department / Functional Area
Key Skills
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