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Clinical Research Associate

Job Description

Job description:- 1. Identify and qualify potential investigators 2. Responsible for identification collection of necessary documents in order to check the feasibility of site/ investigator and approval from authorities. 3. Responsible for training of site study team, recording maintenance of essential documents and for startup activities site initiation. 4. Conduct of monitoring visits to check compliance with study management, protocol other requirements at all assigned sites. 5. Perform source document verification as per monitoring plan and ensure that source documents other trial records are accurate, complete, kept up-to-date maintained according to applicable SOP's to avoid incomplete records. 6. Responsible for study updates Coordination with Labs other trial related services as per the study requirements. 7. Responsible for IP accountability and availability, tracking and management of all Clinical Trial related supplies shipped to the sites/ warehouse accordingly clinical trials supplies vendor management for the study. 8. Responsible for site-closeout follow up activities in order to maintain documents at the site. 9. Assist with the audit of an investigational site or central files and liase with Quality Assurance personnel as required to ensure that the study is being conducted in accordance with ICH GCP and applicable regulatory guidelines. Experience Required: 1 - 4 years

Education/Experience

Job Summary

  • Join WhatsApp Group : Jobs in Ahmedabad
  • Published on: 2020-01-23 02:46:52
  • Last Employer Activity: 2020-01-23 02:46:52

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Clinical Research Associate Jobs in Ahmedabad