Research Assistant

Cynet Systems•Kansas City, KS

4d•Onsite

About The Position

The Research Assistant will be responsible for a variety of tasks related to clinical research studies. This includes verifying and correcting study information, managing data entry into electronic systems, maintaining study files, and assisting with regulatory documentation. The role also involves scheduling subject visits, processing lab specimens, and providing administrative support.

Requirements

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.
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.

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.