Statistical Programmer

6 days ago

bangalore, India Capgemini Engineering Full time

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 status and 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.

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