Require Clinical Research Associate in SIRO Clinpharm
SIRO Clinpharm is one of the leading Global Clinical Research Organizations (CROs), offering full scope services conducting clinical trials in the Pharmaceutical, Biotechnology and Medical Devices sectors in compliance with International Standards. We are headquartered in India having global presence in USA, Israel and in Europe at Germany, Czech Republic, Greece, Estonia, Romania, Spain and France.
Post: CRA / Sr. CRA
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.Conduct site close out. etc.
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. etc
Experience: 2-6 years
Education: B.Pharm, B.Sc
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: CRA
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