Clinical Research Assistant Multiple Locations Available!
This will be an on-site position in the location listed below with a large CRO
Job Description
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.
- Process required lab specimens, label vials, and accurately fill 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.
Qualifications :
- 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
Experience with Patient recruitment, EDC data entry / query resolution,
Job Type
This is a contract position with a duration of 5 Month(s).
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