NOTE -
- Looking for only 7+yeras of experience.
- This Job requires you to work from PAN India Capgemini office.
JOB DESCRIPTION
The Statistical Programmer II (SP II)
- Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR);
- Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies;
- Writes code using Base SAS programs, SAS procedures, or standardized macros;
- Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data;
- Performs data checks as needed, to ensure integrity and correctness of data displays;
- Prepares documentation for programs;
- Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole;
- Creates SAS datasets of clinical data from clinical databases;
- Creates statusand efficacy datasets;
- Creates project-specific macros and formats;
- Loads client data from other platforms and other software packages;
- Prepares data to be sent to clients and as needed for other external transfers and data imports.
- Assists manager and/or director to keep track project timelines and deliverables;
- Leads junior programmers in daily activities and performs on-the-job training to them;
- Communicates with clients for risks, issues, and potential delays
QUALIFICATION FOR ESSENTIAL FUNCTIONS
- Ability to communicate effectively in English, in both writing and verbal.
- Ability to learn quickly and pay attention to details.
- Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries.
- Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients.
- Ability to work independently, takes ownership and strives for quality and efficiency.
- Ability to work positively in a continually changing environment.
- Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.
EDUCATION AND EXPERIENCE REQUIRED
- Bachelor’s degree, but Master’s degree or above, is preferred, in Biostatistics, Computer Science, Mathematics, or a combination of education and relevant industry experiences.
- Strong SAS programming language and good knowledge/experiences of clinical trial and drug development.
- At least 8 years of clinical programming or SAS programming experiences for the SP II position.