Clinical Research Assistant

Clinical Research Assistant Multiple Locations Available!

This will be an on-site position in the location listed below with a large CRO

Locations Available :

Des Moines, IA

Boise, IH

Gurnee, IL

Lafayette, LA

Grand Island, NE

Norfolk, NE

Cleveland, OH

Moore, OK

Austin, TX

Austin,TX

Beaumont, TX

Mesquite, TX

San Antonio, TX

Port Orange, FL

Monroe, NC

Binghampton, NY

East Syracuse, NY

Vestel, NY

East Greenwhich, RI

Spartanburg, SC

Union, SC

Portsmouth, VA

Banning, CA

Long Beach, CA

Modesto, CA

North hollywood, CA

Spring Valley, CA

Collins, CO

Longmont, CO

Las Vegas, NV

Bountiful, UT

Roy, UT

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).