Clinical Research Associate: Site Monitoring & Trials
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Research/Development
Job Description & How to Apply Below
IQVIA is seeking a Clinical Research Associate to perform site monitoring and ensure protocol adherence across study sites. You will manage recruitment plans, training, and regular communications with sites to meet sponsor and regulatory requirements.
Requires 2+ years on-site CRA experience, knowledge of GCP/ICH, and proficiency with EDC/CTMS/eTMF; strong English communication and organizational skills are essential.
Join us at IQVIA Inc as our next Clinical Research Associate:
Site Monitoring & Trials in Afton, WY, United States.
For the Clinical Research Associate:
Site Monitoring & Trials position at IQVIA Inc, we are reviewing applications now.
Step into the Clinical Research Associate:
Site Monitoring & Trials role at IQVIA Inc in Afton, WY, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
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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