Clinical Research Assistant - 246467

Position Overview

The Clinical Research Assistant supports coordinators in the execution of clinical trials, ensuring smooth patient care, accurate data collection, and compliance with study protocols. This is a hands-on role with opportunities to grow into Clinical Research Coordinator and beyond.

Key Responsibilities

• Coordinate and schedule subject visits within protocol windows.
• Prepare visit-specific documentation and charts for the Clinical Research Coordinator.
• Observe and assist coordinators with patient care and management.
• Monitor subject flow and assist in data collection (adverse events, concomitant medications, etc.).
• Transcribe subject information from source documents to Electronic Case Report Forms (eCRFs).
• Administer study questionnaires to participants.
• Conduct and record electrocardiograms (ECGs) per protocol.
• Request medical records for serious adverse event (SAE) reporting.
• Process and ship biological samples for laboratory analysis.
• Perform intraocular pressure checks after injections.
• Conduct trial frame refraction and ETDRS visual acuity testing (for ISTs at selected sites).
• Obtain and document informed re-consent from participants.

Schedule & Compensation

• Hours : Start between 7 : 00–8 : 00 AM, finish 4 : 30–5 : 30 PM (flexible based on needs).
• Pay : $22.00-30.00 (Depending on Experience)