Clinical Research Associate II - Onsite Monitoring
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Research/Development
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Healthcare
Job Description & How to Apply Below
IQVIA Inc is seeking a Clinical Research Associate II with independent on-site monitoring experience to join our team. The candidate will monitor clinical studies across multiple therapeutic areas and ensure compliance with GCP/ICH regulations.
Responsibilities include site visits, training, monitoring progress, and collaboration with cross-functional teams to meet study milestones. Opportunities to support patient recruitment and site administration are available.
We would love to welcome a new Clinical Research Associate II
- Onsite Monitoring to our organisation in Durham, NC, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 75..
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 Clinical Research Associate II
- Onsite Monitoring 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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