Clinical Research Assistant - EMT/LPN/MA/CPhT Preferred

The Clinical Research Assistant (RA) supports the daily execution of clinical trial activities under the guidance of site leadership, the Principal Investigator (PI), and the clinical research staff.  While the PI oversees the conduct of the study and the Clinical Research Coordinator (CRC) manages its day-to-day operations, the RA plays a key supporting role in ensuring protocol compliance and data quality.  Through collaborative efforts with the research team, the RA helps uphold the integrity of the study and prioritizes the safety and well-being of all study participants.Essential Duties and Responsibilities:Including, but not limited to the following:Complete all required site and department training (GCP, IATA, OSHA, SOPs).Maintain exam rooms and manage clinical supply inventory.Ensure trial procedures follow ICH/GCP, federal regulations, site SOPs, and sponsor protocols.Review study protocols and perform delegated tasks (vitals, ECGs, PFTs, phlebotomy, sample processing/shipment, EDC entry, eDiary reconciliation, safety follow-ups).Manage regulatory documentation, lab area upkeep (temperature logs, centrifuge records, inventory), and resolve data queries.Assist with participant screening, scheduling, visit preparation (charts, lab requisitions, kit assembly).Accurately collect and document source data per protocol and GCP standards.Support archiving of study documentation in compliance with regulatory and sponsor requirements.Travel to peripheral/satellite sites to coordinate research activities and oversee visits.