Clinical Research Associate — Site Monitoring Pro
iqviaNew York, NY
Clinical Research Associate — Site Monitoring Pro
iqviaNew York, NY
today
Occupations
Clinical Research CoordinatorsQuality Control AnalystsHealthcare Practitioners and Technical Workers, All OtherIndustries
Other Scientific and Technical Consulting ServicesResearch and Development in BiotechnologyResearch and Development in the Physical, Engineering, and Life SciencesAbout the role
IQVIA Inc in the United States (New Jersey) is seeking a Clinical Research Associate to perform on-site monitoring visits, manage site performance, and ensure protocol adherence per GCP standards. You will coordinate recruitment plans, deliver protocol training, and maintain strong communication with study sites.
The role requires a Bachelor’s degree in a scientific discipline or health care and a minimum of two years’ on-site CRA experience.
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JOB OVERVIEW
Experience level
Mid
Location
New York, NY
Occupation
Clinical Research Coordinators
Industry
Other Scientific and Technical Consulting Services
Posted
today
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