1.To Review of various clinical trial protocols and source documents.
2.Clinical trial data analysis, tagging and updating the database.
3.Advise data management staff on trial parameters, database designs, and validation of
critical data.
4.Reports progress and changes in clinical trials.
5.Statistical analysis and competitive analysis of trial results.
Desired Profile
1.Should have a qualified MBBS, BDS, M Pharm Degree.
2.A strong educational background in clinical research.
3.Computer skills including use of Microsoft word, excel and power point.
4.In depth therapeutic and clinical research expertise as well as knowledge of
GCP/ICH and applicable regulatory guidelines.
Soft Skills
·Client focus
·Result orientation
·Communicating with Impact
·Team player
·Process oriented
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