Dear All now get GMP News, FDA, WHO, EU, TGA, CDSCO guidelines...and GMP Violations news/warning letters.. GMPVIOLATIONS

Wednesday, October 27, 2010

Clinical Trial Analyst -

Job Description
1. 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,

B 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


Experience0 - 3 Years
Industry TypePharma/ Biotech/Clinical Research
RoleClinical Researcher
Functional AreaHealthcare, Medical, R&D
EducationUG - BDS - Dentistry,MBBS - Medicine
PG - M.Pharma - Pharmacy
Compensation:Will match industry standards
KeywordsClinical Trial Analyst, MBBS, BDS, Clinical trials management, clinical research, documentation AE, SAE reporting, designing, clinical trials, ICH - GCP guidelines, ICH - GCP, BA / BE studies, Pharma Analytics
Indegene LifeSystems Pvt Ltd


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