Clinical Research Coordinator

Overview

Seeking a Clinical Research Coordinator in Las Vegas, Neveda

Reports To: Senior Clinical Research Site Manager

Department: Clinical Research Operations

Employment Type: Full-time, onsite, 40 hrs a week

• Collaborate closely with Principal Investigators to coordinate all aspects of assigned clinical studies, including participant recruitment, eligibility assessment, scheduling, treatment coordination, and study-related procedures.
• Perform clinical and study-related procedures, including phlebotomy, vital signs collection, centrifuge operation, ECG administration, and other protocol-required tasks.
• Utilize Microsoft Office and electronic research systems efficiently, including source documentation platforms, IXRS/IWRS, and Electronic Data Capture (EDC) systems such as Medidata, Veeva, and Inform.
• Monitor participant health status throughout the study and promptly communicate relevant findings to the Principal Investigator.
• Identify, document, and report Serious Adverse Events (SAEs) and other safety concerns to investigators and sponsors in accordance with protocol and regulatory requirements.
• Coordinate the collection, processing, packaging, and shipment of biological specimens to designated central laboratories, ensuring accuracy and compliance with laboratory and shipping guidelines.
• Maintain accurate, complete, and organized study documentation in compliance with GCP and regulatory standards.

• Minimum of 3 years of hands-on experience as a Clinical Research Coordinator, preferably in Phase II–IV pharmaceutical clinical trials.
• Bachelor’s degree in a scientific, healthcare, or related field.
• Strong attention to detail with the ability to maintain accurate and well-organized research records.
• Excellent written and verbal communication skills, with the ability to interact professionally with investigators, sponsors, participants, and study team members.
• Working knowledge of ethical principles, regulatory requirements, and GCP guidelines governing clinical research.
• Ability to recognize potential risks, protocol deviations, and adverse events and respond appropriately.