Clinical Coordinator, Non-licensed

University of Virginia

7d

About The Position

The Department of OBGYN is seeking a Clinical Research Coordinator (Varying levels) to join our Benign Gynecology team. A Clinical Research Coordinator 1/2/3/4, Licensed/Non-Licensed (CRC-1, L/NL/ CRC2, L/NL/ CRC-3, L/NL/ CRC-4, L/NL), performs a full range of clinical research duties including working with research participants, processing laboratory specimens, data entry, record keeping, materials preparation, and reviewing of prospective 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 documentation, collect data at all study visits, compile adverse event data, and manage all data collected. 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.
Job Description:
· Recruit, screen, and enroll study participants who meet research criteria for multiple clinical trials.
· Obtain informed consent from study participants and maintain telephone and in-person contact.
· Work closely with Principal Investigators and other study team members on all clinical research projects assigned.
· Notify PI and/or supervisor of any potential issues with the study or subject status.
· Collect subject data, enter and analyze data, and compile reports, adhering to proper research protocols.
· Communicate effectively with study Sponsor(s).
· Prepare documentation, reports, graphs, and other materials. Keep appropriate logs, track participants, and prepare study materials.
· Process, prepare, and ship laboratory specimens.
· In addition to the above job responsibilities, other duties may be assigned.

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
• Clinical Research Coordinator 1, L/NL · Education: Non-licensed trainees possess a Bachelor's degree, and licensed trainees have at least an Associate's degree with an appropriate health-related licensure.
• Clinical Research Coordinator 2, Non-Licensed · Education: Bachelor's degree · Experience: At least one year of clinical research experience.
• Clinical Research Coordinator 2, Licensed · Education: Associate's degree or higher based on medical specialty (with licensure) · Experience: At least one year of clinical research experience.
• Clinical Research Coordinator 3, Non-Licensed · Education: Bachelor's degree · Experience: At least four years of clinical research experience. Related Master's degree may substitute for two years of experience.
• Clinical Research Coordinator 3, Licensed · Education: Associate's degree or higher based on medical specialty (with licensure) · Experience: At least four years of clinical research experience. Related Master's degree may substitute for two years of experience.
• Clinical Research Coordinator 4, Non-Licensed · Education: Bachelor's degree · Experience: At least six years of clinical research experience. Related Master's degree may substitute for two years of experience.
• Clinical Research Coordinator 4, Licensed · Education: Associate's degree or higher based on medical specialty (with licensure) · Experience: At least six years of clinical research experience. Related Master's degree may substitute for two years of experience.

Nice To Haves

• Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is preferred at the time of hire and is required within one year.

Responsibilities

• Recruit, screen, and enroll study participants who meet research criteria for multiple clinical trials.
• Obtain informed consent from study participants and maintain telephone and in-person contact.
• Work closely with Principal Investigators and other study team members on all clinical research projects assigned.
• Notify PI and/or supervisor of any potential issues with the study or subject status.
• Collect subject data, enter and analyze data, and compile reports, adhering to proper research protocols.
• Communicate effectively with study Sponsor(s).
• Prepare documentation, 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
• Number of Employees: 5,001-10,000 employees