** 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
Position Overview
The Clinical Research Coordinator (CRC) plays a key role in the successful execution of clinical research studies by supporting investigators and ensuring studies are conducted in compliance with protocol requirements, Good Clinical Practice (GCP), and applicable regulatory guidelines. This position involves direct participant interaction, study coordination, and accurate documentation throughout all phases of clinical trials.
Key Responsibilities
-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.
Qualifications
-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
promptly and appropriately.
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