Research Assistant

Job Description

Job Description

The research coordinator is responsible for coordinating research patient visits according to the ICH-GCP guidelines and the IRB-approved study protocol and / or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization, which are subject to change from time to time.

Compensation : $20 hourly

Responsibilities :

• Coordinate and schedule subject visits within study / subject-specific windows per protocol guidelines
• Prepare visit-specific documentation and charts for the Clinical Research Coordinator
• Observe the Coordinator in patient care and management
• Assist the 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 subjects, and conduct electrocardiograms (ECG) on subjects as required per the 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 regarding ICFs
• Perform other duties as assigned
• Obtain any applicable additional / required sponsor training and / or certification

Qualifications :

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