Source description
About the role
Location - Pune, Mumbai, Thane, Bengaluru, Hyderabad, Greater Noida Experience in statistical programmers for a compound/indication or therapeutic area Proficiency in SAS / R programming languages to Program and validate SDTM, ADAM, TFL and statistical analyses In-depth understanding of SAS programming concepts and techniques in drug development process and clinical study life cycle Good to have experience in other statistical programming languages (R) In-depth understanding of CDISC standards and therapeutic area (Oncology, Immunology, Neuroscience etc) Experience with regulatory filings Ability to effectively represent the Statistical Programming Organization in cross functional teams (Statisticians, Clinical Data Management, Medical Writing, Regulatory Publishing and Clinical Operations) Must Have Skills - SAS, Statistical Analysis, SDTM, ADAM, TLF .
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