Research Assistant

Overview

Clinical Research Recruiter Advisor @ Medix™ | Building relationships within Clinical Research

Note: This description reflects a role for a Clinical Research Coordinator at a known site in Salt Lake City, Utah.

$52,000.00/yr - $54,000.00/yr

• 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 Coordinator in patient care and management.
• Assist Coordinator in monitoring subject flow and subject care and management.
• Observe, assist, collect and record all necessary data for follow up (e.g., adverse events, concomitant medications) for 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 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 with regard to ICFs.
• Perform other duties as assigned and obtain any applicable additional/required sponsor training and/or certifications.

• Not Applicable

• Full-time

• Research

• Research Services

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Note:

The following items are present in the original description for context but are not required for the core job specification and are omitted here to maintain focus on role responsibilities and qualifications.