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