Required Attributes : Graduate/ Masters in Life Science, B Pharma/ M/ Pharma with minimum 4 years of experience. Key responsibilities:1. Independently develop and finalize documents of the study, and scientific documents for different regulatory submissions such as study protocol and EC documents. Bioanalytical reports, Clinical Study Reports (CSRs), part of Electronic Common Technical Document (eCTD) modules covering various therapeutic areas, and phases
Required Attributes : Graduate/ Masters in Life Science, B Pharma/ M/ Pharma with minimum 4 years of experience. Key responsibilities:1. Independently develop and finalize documents of the study, and scientific documents for different regulatory submissions such as study protocol and EC documents. Bioanalytical reports, Clinical Study Reports (CSRs), part of Electronic Common Technical Document (eCTD) modules covering various therapeutic areas, and phases
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