Clinical Research Monitor: Site & Sponsor Alignment
IQVIA
IQVIA is seeking an on-site Clinical Site Monitor in Kansas to ensure sites conduct studies per protocol and regulatory guidelines. You will perform monitoring visits, train site staff, and manage documentation across TMF/ISF while tracking enrollments and data quality. The role requires 1+ year of on-site monitoring, strong English communication, and proficiency in MS Office; collaboration with study teams is essential. Base pay varies with experience. #J-18808-Ljbffr IQVIA
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Clinical Research Monitor: Site & Sponsor Alignment in Overland Park, KS vacancy
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Sr. CRA, Sponsor Aligned, Oncology page is loaded## Sr. CRA, Sponsor Aligned, Oncologylocations... ...Overview: Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study...WebsiteFull timePart timeWork at officeLocal areaImmediate startWorldwide$74.5k - $175.1k
Job OverviewPerform monitoring and site management work to ensure that sites... ...regulations and guidelines, and sponsor requirements.Essential... ...regulatory requirements, i.e., Good Clinical Practice (GCP) and... ...applying, applicable clinical research regulatory requirements (i.e...WebsiteFull timePart timeLocal areaImmediate startWorldwideIQVIA
Overland Park, KS3 days ago- IQVIA is seeking a Clinical Research Associate to perform monitoring and site management to ensure sites conduct studies and report data per protocol, regulations, and sponsor requirements. Responsibilities include site visits, recruitment tracking, training, communication...Website
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...IQVIA seeks a Clinical Research Associate to conduct site monitoring and management for clinical studies. The role ensures sites comply with protocols, regulations, and sponsor requirements while managing recruitment, data quality, and study documentation. Responsibilities...WebsiteWork at office- A leading clinical research organization is seeking a Clinical Research Associate dedicated to supporting... ...should have 1-2 years of onsite monitoring experience, a bachelor's degree in a... ...regulatory requirements. The role involves site monitoring visits, ensuring compliance...Website
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MCRA, LLC
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Kansas City Card Arrhythmia Research
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