Senior Statistical Programmer / Analyst III

Job description

**Responsibilities:** - Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. - Develop SDTM specifications and generate SDTM datasets using SAS; - Develop ADaM,specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan; - Develop Tables, Listings, Graphs, Patient Profile in support of the Clinical Study Report, Posters, Manuscripts; - Develop ADaM data, Tables, Listings, Figures for Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE) - Create electronic submission packages to FDA, e.g., define.xml or define.pdf following FDA guidelines with no supervision. - Expert-level in analyze information and develop innovative solutions to programming and data analysis challenges; - Serve as point of contact (POC) of programming with statisticians for statistical input and analysis interpretation; - Follow and reinforce regulatory agency requirements during daily job. - Serve as a programming team lead and contribute to department initiatives. - Provide guidance, mentoring, training for team members and help solve issues from cross-functional teams; - Review draft and final production deliverables for project to ensure quality and consistency. - Work with global team or sponsors to coordinate project deliverables, timelines and resources. **Skills and Responsibilities:** - Bachelor’s/Master’s degree in Statistics, Mathematics, Computer Science, Electrical Engineering, Biotechnology or related scientific disciplines with 5+years of clinical programming experience. - Proven knowledge and training in high level computing languages such as. SAS, C/C++, Java, R, Python, MATLAB and SQL. Database programming experience is a plus. - Expert-level in decoding programming logic and assembling programming code based on logic provided and be able to explain to team members. - Expert level in applying concept in Artificial Intelligence and Machine Learning in real world. - In-depth knowledge of ICH, Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology. - Good understanding of clinical drug development process. - Strong communication skills and coordination skills; ability to communicate with global teams independently. - In-depth understanding of clinical drug development process. - Detail-oriented and ability to learn and adapt to changes.