Posted:2 weeks ago|
Platform:
Work from Office
Full Time
Role & responsibilities Developing, testing, validating, and maintaining SAS programs to generate analysis datasets, tables, listings, and figures Working closely with data management and statistical teams to understand the requirements for each project Reviewing clinical trial data and addressing any data inconsistencies or errors Designing and implementing strategies to manage, clean and verify clinical trial data Performing statistical analysis on clinical trial data Creating and maintaining documentation for all SAS programs and processes Ensuring that all programming activities and processes performed are conducted according to standard operating procedures and good programming practices Contributing to the development of standard operating procedures, guidelines, and best practices for SAS programming Assist with the development of statistical analysis plans. Provide input into clinical trial protocols and case report forms. Ensure data consistency and integrity. Meet project timelines and deliverables. Additional: Knowledge of CDISC SDTM and ADaM data models. Qualifications Proven work experience as a Clinical SAS Programmer. Experience in developing and validating SAS programs in a clinical research environment. Strong statistical analysis skills. Attention to detail and problem-solving skills. Proficient in the use of SAS Macro language and other advanced SAS features. Excellent written and verbal communication skills. BSc or higher degree in Statistics, Mathematics, Computer Science or a related field Interested Candidates please send me updated resumes to pitchireddy.t@hetero.com
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