Tuesday, March 30, 2010

Bangalore, Hyderabad; Clinical Research Associate; B.Pharm, M.Pharm; Parexel

Description:
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.

Experiance: 2-3 years

send resumes to: kirloskar.das@parexel.com