Expert SAS Programmer Lead

2 days ago

Kota, Rajasthan, India beBeeDataAnalyzer Full time ₹ 1,50,00,000 - ₹ 2,00,00,000

Senior Statistical Programmer

  • We are seeking a highly skilled SAS Programmer to join our team as a Senior Statistical Programmer. As a member of our team, you will be dedicated to one of our global pharmaceutical clients and work at the heart of their innovation.
About this role
  • This is an exciting opportunity for you to contribute your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials.
Responsibilities
  • You will leverage your expertise to perform data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming.
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
  • Production and QC/validation programming.
  • Generating complex ad-hoc reports utilizing raw data.
  • Applying strong understanding/experience of Efficacy analysis.
  • Creating and reviewing submission documents and eCRTs.
  • Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries.
  • Performing lead duties when called upon.
Requirements
  • Bachelor's degree in one of the following fields Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 5 years of related experience with a master's degree or above.
  • Study lead experience, preferably juggling multiple projects simultaneously preferred.
  • Strong SAS data manipulation, analysis, and reporting skills.
  • Solid experience implementing the latest CDISC SDTM / ADaM standards.
  • Strong QC/validation skills.
  • Good ad-hoc reporting skills.
  • Proficiency in Efficacy analysis.
  • Familiarity with drug development life cycle and experience with the manipulation, analysis, and reporting of clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.
What we offer
  • We believe in applying scientific rigor to reveal the full promise inherent in data.
  • We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
  • We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

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