Company Name : Siro Clinpharm
Qualification : Doctorate/Master’s/Bachelors Degree in Science
Location : India
Experience : Minimum 2 Yr.
Job Description :
*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.
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.
For original notification Click Here
No comments:
Post a Comment