Senior Statistician

SGSHyderabad, Telangana, IndiaonsiteSalary not postedView the original posting at SGS ↗

Responsible for providing statistical support in the clinical research, including monitoring and querying data from the database, managing study data, executing the statistical analysis, providing statistical reports, validating statistical analysis. Will also involve in reviewing research protocol drafts and the report draft, and in assisting the statistics manager in the design of appropriate statistical analysis plans and keep track of due dates. Will be responsible to answer sponsors' questions when the statistics manager is not available. At all times, complies with SGS Code of Integrity and Professional Conduct. Develop and program statistical analysis plans Perform statistical programming and validation of analyses and data listings Present statistical results and prepare reports Provide consulting and support to clients Enhance and maintain SAS macros for standardized evaluations Contribute to the development of innovative process improvements Provide functional and disciplinary leadership to two team members Ensure full knowledge of, and adherence to, SGS procedures, guidelines, and quality standards. Ensures work area in GBS is kept clean and presentable at all times. Remains familiar with SGS quality assurance procedures. Complies to all SGS QHSE and HR policies and procedures **Required Qualifications:** Bachelor of Science (B.Sc) in Mathematics, Statistics, Biology, or a related quantitative discipline Master of Science (M.Sc) or equivalent postgraduate qualification in Mathematics, Statistics, Biology, or related field Minimum 3 years of professional experience in statistical analysis, preferably within clinical research or pharmaceutical environments Proficiency in SAS programming for statistical analysis and data manipulation Strong knowledge of statistical methodologies and clinical trial design principles Demonstrated experience in data validation and quality assurance processes At least 5 years of clinical research experience in pharmaceutical or Contract Research Organization (CRO) industry, including 3 years of Statistical Programming of TLFs. Experience in writing SAPs and acting as study statistician

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