Clinical Research Associate - Site Monitoring; Oncology
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Research/Development
Job Description & How to Apply Below
Parexel is seeking a Clinical Research Associate to act as the primary contact and site manager for oncology and multi-specialty trials across US West/Central locations. The role emphasizes strong site relationships, regulatory adherence, and data integrity throughout all trial phases.
Responsibilities include remote and on-site monitoring, regulatory documentation management, and collaboration with sponsor teams to ensure site readiness. Domestic/international travel may be required.
The Clinical Research Associate
- Site Monitoring (Oncology) role at Parexel is now open for applications in Carson City, NV, United States.
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
- Site Monitoring (Oncology) role in the description above.
We appreciate your interest in this position.
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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