Senior Clinical Research Associate I — Site Monitoring Pro
IQVIA
IQVIA is hiring Senior Clinical Research Associate 1 with experience across multiple therapeutic areas to monitor and manage trial sites, ensuring protocol adherence and data integrity. The role emphasizes on-site monitoring, regulatory tracking, and collaboration with study teams in a global clinical research environment. The position involves training sites, coordinating with investigators, and maintaining essential TMF/ISF documentation, with potential involvement in start-up activities and #J-18808-Ljbffr IQVIA
Vacancy posted 3 days ago
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Overland Park, KS3 days ago$74.5k - $197.5k
...country where the job is located.Perform monitoring and site management work to ensure that sites... ...contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive... ...in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical...SeniorWebsiteFull timePart timeLocal areaImmediate startWorldwideIQVIA
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Myana is looking for Clinical Research Associates at the CRA 2 level. The ideal candidate should have 1-2 years of onsite monitoring experience in Cardiovascular/Renal/Metabolic, Oncology, or Neurology. This position involves site monitoring visits and ensuring compliance...Website- IQVIA is seeking a Clinical Research Associate to ensure study sites operate smoothly and efficiently, advancing groundbreaking oncology research. You will... ...BS in a scientific field, 1+ year on-site oncology monitoring experience, and strong communication and organizational...Website
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$90.2k - $175.1k
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Shawnee, KS1 day ago $74.5k - $197.5k
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The Phoenix Group
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