Senior Clinical Research Associate — On-Site Monitoring Lead
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Research/Development
Job Description & How to Apply Below
IQVIA is seeking a Senior Clinical Research Associate 1 with experience across oncology, cardiovascular, renal, metabolic, CNS, obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory. The role focuses on monitoring sites to ensure studies are conducted per protocol, regulatory requirements, and sponsor standards.
The Senior CRA 1 will perform site visits, coordinate site training, manage regulatory submissions, and maintain TMF/ISF documentation while collaborating with study
For the Senior Clinical Research Associate — On-Site Monitoring Lead position at IQVIA Inc, we are reviewing applications now.
This opportunity is part of our work in Management & Operations.
The advertised compensation is 90..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Clinical Research Associate — On-Site Monitoring Lead role in the description above.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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