A Clinical SAS Analyst is responsible for utilizing SAS software to analyze and manage clinical trial data, generating tables, listings, and figures for reports, while ensuring data integrity and compliance with regulatory guidelines by collaborating closely with biostatisticians and data managers throughout the clinical research process;.
Key responsibilities:
Data Cleaning and Manipulation
Develop and execute complex SAS programs to generate analysis datasets, tables, listings, and figures according to the Statistical Analysis Plan (SAP) and study protocol.
Perform statistical analyses on clinical trial data using appropriate SAS procedures, including descriptive statistics, hypothesis testing, and regression analysis.
Perform statistical analyses on clinical trial data using appropriate SAS procedures, including descriptive statistics, hypothesis testing, and regression analysis.
Conduct data quality checks to identify and resolve data discrepancies, ensuring data integrity throughout the analysis process.
Create clear and concise clinical study reports, including tables, listings, and figures, for interim and final analysis, adhering to regulatory standards.
Work closely with biostatisticians, data managers, clinical trial teams, and other stakeholders to design analyses, interpret results, and address data issues.
Qualifications
Master's degree in biostatistics, statistics, or a related field
Minimum of 0-2 years of experience in clinical SAS programming
Strong understanding of statistical analysis methods
Experience working with clinical trial data.
Excellent SAS programming skills
Proficient in data manipulation techniques
Strong communication and interpersonal skills
Ability to work independently and as part of a team.
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Employement Category:
Employement Type: Full timeIndustry: Medical / HealthcareRole Category: Pharmacist / Medical RepresentativeFunctional Area: Not SpecifiedRole/Responsibilies: Clinical SAS Analyst