Mumbai; Clinical Research Associate; B.Pharm, M.Pharm; Siro Clinpharm Pvt Ltd

Location
Mumbai
Experience
2 - 4 years
Education: B.Pharm, M.Pharm

Job Description

The core responsibilities for the position would be Site Monitoring.

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.


send resumes to: hr@siroclinpharm.com