Medix™
**Seeking a Clinical Research Assistant in Nashville, TN**
Read all the information about this opportunity carefully, then use the application button below to send your CV and application.
Location: Nashville, TN Schedule: Monday - Friday; 8:00AM - 4:30PM CST Employment: Contract to Hire Pay Rate: Level I- $18-$24 hourly Level II- $20-$26 hourly Level III- $22-$28 hourly
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 ICF’s • Perform other duties as assigned • Obtain any applicable additional/required sponsor training and/or certifications
Read all the information about this opportunity carefully, then use the application button below to send your CV and application.
Location: Nashville, TN Schedule: Monday - Friday; 8:00AM - 4:30PM CST Employment: Contract to Hire Pay Rate: Level I- $18-$24 hourly Level II- $20-$26 hourly Level III- $22-$28 hourly
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 ICF’s • Perform other duties as assigned • Obtain any applicable additional/required sponsor training and/or certifications