Job Designation- Clinical Research Associate.
Job Description-Ensure all assigned studies follow SIRO/applicable SOPs, GCP and local regulations. To do all regulatory/ethics submission as per timelines and to ensure regulatory documents are available, complete and current.In coordination with the project manager and/or medical monitor, perform study site qualification visits. Also to participate in/conduct investigator�s meeting and site initiation visits. To identify, define, coordinate and conduct site study training.To prepare monitoring reports.To maintain audit readiness at the site level.
Requirements - Pharmacy,At least 1 yr of monitoring experience of handling clinical trials in Phase I, II, III & PMS (Post marketing studies).
Contact details-Ms.Deepti Kshirsagar,
Siro ClinPharma Pvt.ltd
Telephone:022-25848000
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