Become a vital contributor as a Statistical Programming Specialist in clinical trials. Develop and validate datasets, ensuring data integrity and compliance in a dynamic research environment.

You'll be responsible for programming SDTM and ADaM datasets and crafting SAS output for clinical study reports. Collaborate with Data Managers to enhance data quality during trials and support the overall integrity of the research process. Ideal candidates will have a strong background in statistics and bioinformatics.

Key Responsibilities: • Develop specifications for statistical datasets • Validate datasets and perform compliance checks • Generate SAS programming for trial statistics • Conduct data integrity checks and rectifications • Document programming processes thoroughly

Requirements: • Master’s or Ph.D. required in relevant discipline • SAS certification (Base/Advanced) is a must • Experience in statistical programming in clinical trials preferred • Excellent p...