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2.0 - 6.0 years

0 Lacs

haryana

On-site

Role Overview: As a Clinical Research Associate (CRA), you will be responsible for performance and compliance for assigned protocols and sites in a specific country. Under the guidance of the CRA-Manager, you will ensure the adherence of study conduct to ICH/GCP and country regulations, company policies and procedures, quality standards, and reporting requirements for adverse events internally and externally. Your primary role will involve acting as the main point of contact and site manager throughout all stages of a clinical research study, assuming overall responsibility for allocated sites. You will actively contribute to the development and expansion of the territory for clinical resear...

Posted 1 month ago

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