Senior SAS Programmer

Job Title: Senior SAS Programmer

Location

Employment Type

Experience

Job Summary:

Senior SAS Programmer

Key Responsibilities:

• Perform

  data manipulation, analysis, and reporting

  of clinical trial data, including both safety and efficacy datasets (ISS/ISE), using

  SAS

  .
• Generate and validate

  SDTM and ADaM datasets

  in accordance with CDISC standards.
• Create and validate

  Tables, Listings, and Figures (TLFs)

  for study reports and regulatory submissions.
• Develop

  complex ad-hoc reports

  from raw clinical data.
• Apply a strong understanding of

  efficacy analyses

  and clinical endpoints.
• Contribute to the preparation and review of

  submission documents

  and

  electronic Case Report Tabulations (eCRTs)

  .
• Perform

  production programming

  and

  quality control (QC/validation)

  to ensure accuracy and consistency.
• Act as a

  team player

  , demonstrating commitment to quality and meeting project deadlines.
• Stay

  adaptable and flexible

  to shifting priorities in a fast-paced clinical environment.

Required Qualifications:

• Bachelor’s or Master’s degree in

  Life Sciences, Statistics, Computer Science

  , or a related field.

• 7+ years

  of hands-on experience in

  clinical trial programming

  using

  SAS

  .
• Proficient in

  CDISC standards

  (SDTM, ADaM), including mapping and validation.
• Strong working knowledge of

  Base SAS, SAS Macros, SAS/STAT, and SAS/GRAPH

  .
• Experience in generating datasets and outputs for

  regulatory submissions

  (including ISS/ISE).
• Familiarity with

  eCTD standards

  , including

  Define.xml

  and dataset documentation.
• Excellent attention to detail and strong analytical problem-solving skills.

Why Join Us?

Join a collaborative team environment where your expertise in clinical data programming directly contributes to advancing global healthcare. We value precision, integrity, and innovation in every project we undertake.