**Seeking a Clinical Research Assistant in Nashville, TN**
Location: Nashville, TN
Schedule: Monday - Friday; 8:00AM - 4:30PM CST
Employment: Contract to Hire
Pay Rate:
Duties:
Coordinate and schedule subject visits within study/subject specific windows per protocol
guidelines.
Prepare visit-specific documentation and charts for Clinical Research Coordinator
Observe Coordinator in patient care and management
Assist Coordinator in monitoring subject flow and assist in subject care and management
Observe, assist, collect and record all necessary data for follow up (e.g. adverse events, concomitant
medications, etc.) study visits (Phase 2 & 3; NO Gene Therapy)
Transcribe subject study information from source documents to the Electronic Case Report Forms
Administer all mandatory questionnaires to study subjects
Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects as required per study
protocol
Promptly request all necessary medical records for Serious Adverse Event Reporting
Process and ship laboratory biological samples for analysis
Perform intraocular pressure checks after injections
Perform trial frame refraction and ETDRS visual acuity testing (For ISTs only, at selected sites)
Inform subjects and obtain written re-consents in regard to ICFs
Perform other duties as assigned
Obtain any applicable additional/required sponsor training and/or certifications
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