Tuesday, June 21, 2011

Job : Clinical Research Associate (CRA) - Siro Clinpharm

Company Name : Siro Clinpharm
Qualification : Doctorate/Master’s/Bachelors Degree in Science
Location : India
Experience : Minimum 2 Yr. 
Job Description : 

*Perform study site qualification visits, participate/conduct investigator’s meeting and site initiation visits in coordination with the project manager and/or medical monitor

*To ensure all assigned studies follow SIRO/applicable SOPs, GCP and local regulations. Ensure regulatory documents are available, complete and current and submitted as per timelines.

*To identify, define, coordinate and conduct site study training. Perform regular monitoring visits to site, prepare monitoring reports and maintain audit readiness at the site level.

*Responsible for recruitment and propose alternative solutions if the predefined objectives are not met, either in the terms of patient number or timelines.

*To resolve all data queries or other study related queries from the site within timeframe.

*Conduct site close out and assure appropriate archival of controlled documents.
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