Job detail

Non-licensed Clinical Research Coordinator 1, Surgery

University of Virginia

#Vital Signs #Healthcare #Surgery #Medical History #Data Management #Non-exempt #Clinical Research #Clinical Trials #IRB

Quick overview

The coordinator will manage clinical trial activities, including recruiting and consenting participants, collecting and analyzing study data, and processing laboratory specimens. They are also responsible for maintaining study documentation and submitting protocols to the Institutional Review Board.

Requirements summary

A Bachelor's degree or an equivalent combination of experience and education is required. While no prior experience is mandatory, knowledge of medical terminology or experience in a healthcare setting is preferred.

bachelor degreeWritten CommunicationRecord KeepingProblem SolvingMedical TerminologyMedical AssessmentOral CommunicationOrganization SkillsData CollectionPatient RecruitmentSymptom ManagementInformed ConsentPatient ScreeningIRB SubmissionClinical Trial CoordinationLaboratory Specimen ProcessingBiomarker Collection

Job description

The Department of Surgery is seeking a Clinical Research Coordinator 1, Non-Licensed to conduct a variety of clinical trial activities.
Duties will include working with research participants, processing laboratory specimens, document preparation, record keeping, materials preparation, and reviewing of prospective research participants.
The incumbent will 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.
Additionally, the incumbent is expected to complete on call rotations.
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.
Additionally, qualified candidates must be able, with training, to collect, process and ship biomarkers, including blood and other body fluids.
Job Responsibilities Include: Recruit, screen, and enroll study participants who meet research criteria.
Collect basic information through scripted interviews and answer general questions.
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 documentation, reports, graphs, and other materials.
Keep appropriate logs, track participants, and prepare study materials.
Process, prepare and ship laboratory specimens.
Submit study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor.
Obtain medical histories and conduct medical assessments of clinical trial subjects, including symptom management with appropriate referral.
Create treatment plans and serve as an information resource for trial subjects.
Perform physical exams, including assessing vital signs and administering prescribed medications.

Non-licensed Clinical Research Coordinator 1, Surgery

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