Lead SAS Programmer for Clinical Trials

4 days ago


Pune, Maharashtra, India Lifelancer Full time

Job Overview

We are seeking a highly skilled Lead SAS Programmer to join our team at Lifelancer. As a key member of our pharmaceutical clients' innovation team, you will leverage your advanced SAS programming skills and proficiency in CDISC standards to support or lead one or more Phase I-IV clinical trials.

Key Responsibilities

  • 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 internal cross-functional teams and clients for project specifications, status, issues, or inquiries

Requirements

  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 8 years of SAS programming experience working with clinical trial data in the Pharmaceutical Biotech industry
  • Study lead experience, preferably juggling multiple projects simultaneously
  • 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 manipulating, analyzing, and reporting clinical trials' data

Salary Range

$120,000 - $180,000 per year, depending on experience

About Us

Lifelancer is a talent-hiring platform connecting professionals with opportunities in Life Sciences, Pharma, and IT. We value scientific rigor, collaboration, and innovation in our work.



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