Clinical Research Coordinator (Varying Levels), Clinical Trials Unit

University of Virginia

1d • Onsite

About The Position

The School of Medicine Clinical Trials Unit at the University of Virginia is seeking a Non-licensed OR Licensed Clinical Research Coordinator (varying levels) to conduct a variety of clinical trial activities. Duties will include interacting with research participants, processing laboratory specimens, entering data, maintaining study records and screening of potential research participants. Clinical Research Coordinators will also assist with clinical trial-related activities, recruit, screen, and consent potential study participants, schedule study visits, prepare and maintain study regulatory documentation, collect data at study visits, compile adverse event data, manage all data collected, communicate with ancillary personnel involved with the study, and collaborate with the study sponsor representatives. Individuals seeking this position must have strong organization skills, have the ability to problem-solve, work well in a team environment, have excellent written and oral communication skills, strong assessment skills and demonstrate an ability to learn new information quickly.

Requirements

• strong organization skills
• ability to problem-solve
• work well in a team environment
• excellent written and oral communication skills
• strong assessment skills
• demonstrate an ability to learn new information quickly
• Bachelor's Degree Required or equivalent combination of experience, education and or certifications.

Nice To Haves

• Clinical Research Coordinator (CCRC)
• Certified Clinical Research Professional (CCRP)
• Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.

Responsibilities

• Recruit, screen, and enroll study participants who meet research criteria for multiple clinical trials in the School of Medicine.
• Ensure study procedures are conducted in compliance with research protocol.
• Obtain informed consent from study participants and maintain telephone and in-person contact. Notify Principal Investigator and supervisor of subject status.
• Collect subject data, enter and analyze data, and compile reports, adhering to proper research protocols.
• Prepare and submit regulatory documents to appropriate review committees as per federal, state and local regulations and institutional policies
• Prepare reports, graphs, and other materials. Keep appropriate logs, track participants, and prepare study materials.
• Process, prepare, and ship laboratory specimens.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level