Senior Statistical Programmer / Analyst III

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.