Research Assistant

24 hours per week

Job Overview
Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies.

Essential Functions

• Provide clinical research support to investigators and site staff, including
• 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.
• Prescreen referrals and patient recruitment
• Collect and submit regulatory/ethics documentation pertaining to the research study.
• Maintain the FDA 1572 form for assigned research studies.
• 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.

Qualifications

• High School Diploma or equivalent High School Diploma Req
• Basic knowledge of clinical trials
• Clinical Research Coordinator experience
• In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
• Basic knowledge of medical terminology
• Basic skill in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
• Excellent interpersonal skills
• • Ability to pay close attention to detail
• • Ability to establish and maintain effective working relationships with coworkers, managers and clients
• • Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies Upon Hire Req?