Statistical Programmer I

2 days ago


Clark Freeport Zone Pampanga Philippines HiPaaS, Inc. Full time $80,000 - $120,000 per year

Job Description:

  • 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.

In addition to the above job duties, SP II also

  • · Assists manager and/or director to keep track of project timelines and deliverables;
  • Leads junior programmers in daily activities and performs on-the-job training for them;
  • Communicates with clients about risks, issues, and potential delays.

QUALIFICATION FOR ESSENTIAL FUNCTIONS

  1. Ability to communicate effectively in English, both in writing and verbally.

  2. Ability to learn quickly and pay attention to details.

  3. Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on-time deliveries.

  4. Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients.

  5. Ability to work independently, take ownership, and strive for quality and efficiency.

  6. Ability to work positively in a continually changing environment.

  7. Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and their implications to drug development.

EDUCATION AND EXPERIENCE REQUIRED

  1. Bachelor's degree, but Master's degree or above, is preferred, in Biostatistics, Computer Science,

Mathematics, or a combination of education and relevant industry experience.

  1. Strong SAS programming language and good knowledge/experience of clinical trial and drug

development.

  1. At least 2 years of clinical programming or SAS programming experiences for the SP II position.

WORK REQUIREMENTS

  1. Corporate office environment.

  2. Some travel (5%) may be required, with a potential of travel occurring over weekends.

  3. Cross-functional interactions.

TRAINING

  • · Complete Training Requirements per the current Training Requirements List.
  • The supervisor will assign additional skills training, one-on-one, see-one / do one, or other Training as necessary to achieve qualifications and improve job performance.


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