Statistical Analyst II

Responsibilities • Demonstrated practical understanding of SAS programming concepts and techniques appropriate to the pharmaceutical industry. • Demonstrated satisfactory ability to apply SAS programming knowledge and work independently to solve problems related to non-routine situations. • Responsible for the creation and validation of ADaM, TLFs for CSR, ISS, and Client following's SOPs, department, and project standards. • Responsible for the accuracy of SAS programs by reviewing output, reviewing code, reviewing log files and resolving Pinnacle 21 checks. • Responsible for the creation and accuracy of derivations as defined in the protocol and statistical analysis plan. • Demonstrated satisfactory ability to interpret statistical analysis plans to develop analysis data set specifications. • Ensure consistency across studies within a project. • Responsible for the creation of data definition documents, TOCs, and support submission related activities. • Learn and maintain expertise in the use of the utilities and macros developed for the Statistical Programmers. • Develop new macros and utilities. Requirements • MS in Statistics, Computer Science or a related field with 5 to 7 years of SAS programming experience in Pharmaceutical or related industry OR. • BS in Statistics, Computer Science or a related field with 5 to 7 years of SAS programming experience in Pharmaceutical or related industry. • Strong experience with clinical trials, including familiarity with expectations of regulatory agencies, • Strong working experience/skill in ADaM datasets creation/validation. • Strong technical and communication skills, both oral and written. • Competent in SAS programming, macro, and utilities development. • Good CDSIC knowledge. • Provide accurate and timely responses to requests from clients with a sense of urgency. • Be compliant with training requirements.