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Research Assistant
Indianapolis, IN
2 months assignment
Summary:
A typical Research Assistant performs a variety of administrative tasks in support of clinical trials and assists in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.
Responsibilities
Verify and/or correct research study information on source documents. Research queries and variances, and provide feedback to the site data collector
Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness
Prepare and maintain research study files
Compile, collate and submit study information within established deadlines
Assist in maintenance of regulatory documentation
Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits
Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget
Processing of required lab specimens, labeling of vials, and accurately filling out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations
Perform various administrative support functions such as reception, office organization, and office supply management
Skills
Basic knowledge of clinical trials
In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
Excellent interpersonal skills
Education/Experience
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting; e.g. clinical research coordinator, nurse, medical assistant
