Part Time Clinical Research Coordinator - Florence, SCThis is a contract position and requires previous clinical research experienceJob Description:Looking to hire an onsite part time individual with clinical research experience to act as a consultant CRC to support an ongoing Lupus clinical trial. This CRC must be experienced in being able to work independently. You will act as one of the main CRC’s for this study. A candidate must help the site and study wherever needed depending on the specific assignment.Short term contract, 16hrs/week.Responsibilities:
Patient recruitment
Chart review of patient medical records
Phone screening
Informed consent
Collection of study data and entering into EDC
Resolving queries
Regulatory
Scheduling for in-patient visits
Scheduling follow up appointments
Appointment reminders
Any study efforts deemed necessary by the site
Qualifications:
Minimum of two years in a Clinical Research Coordinator role
Experience with electronic medical records (EMR)
Experience with electronic data capture (EDC) systems
Experience working in regulatory
Bilingual in Spanish & English (preferred)
Recruiter: Shelby Ciardelli
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