Senior Statistician Professional

SGS India; Hyderabad; On-site; INR 1,200,000 - 2,000,000; Full time

Job summary

SGS India is seeking a skilled statistician to provide statistical support for clinical research, monitor data, and execute analyses. You will validate analyses, generate reports, and review protocol drafts while assisting in SAP design.

You will answer sponsor questions when the statistics manager is unavailable and contribute to process improvements. The role requires 3+ years in statistical analysis, strong SAS programming, and 5+ years in clinical research within pharma/CRO settings;

Qualifications

• BS in Mathematics, Statistics, Biology or related quantitative field.
• MS or equivalent in Mathematics, Statistics, Biology or related field.
• 3+ years of professional experience in statistical analysis.
• Proficiency in SAS programming for statistical analysis.
• 5+ years of clinical research experience in pharma/CRO environments.

Responsibilities

• Provide statistical support in clinical research, including monitoring and querying data from the database.
• Execute statistical analyses and generate statistical reports.
• Validate statistical analyses and data listings.
• Review research protocol drafts and report drafts; assist in SAP design.
• Answer sponsor questions when the statistics manager is unavailable.

Skills

SAS programming

Statistical analysis

Data validation

Quality assurance

Clinical trial design

Team leadership

Education

B.Sc in Mathematics/Statistics/Biology

M.Sc or equivalent

Tools

SAS

SAS macros

Job description

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 Qualifications

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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