Bachelor's degree in life sciences, nursing, pharmacy, or a related medical/scientific discipline, or an equivalent combination of education, training, and relevant experience.
3-5+ years of independent clinical monitoring experience as a CRA, including demonstrated experience conducting site qualification, initiation, interim monitoring, and close-out visits.
Strong medical and scientific knowledge, with demonstrated ability to independently review and interpret clinical source documentation, including medical histories, laboratory results, concomitant medications, adverse events, and eligibility criteria.
Must be based in the Las Vegas, NV area to support the primary investigational site, with flexibility to travel to additional locations as needed.
Valid driver's license where applicable.
Thorough understanding of ICH-GCP, applicable regulations, SOPs, and clinical monitoring requirements.
Proficiency in Microsoft Office and the ability to learn and effectively utilize clinical trial management systems and other relevant software.
Strong English language and grammar skills.
Location Requirement: Candidates must be based in the Las Vegas, NV area, as this position will primarily support an investigational site in that location.
Regular travel to the primary Las Vegas investigational site is required, with potential travel to additional sites in other locations based on study assignments and business needs.