Clinical Trials Data Analyst Leader

6 days ago

Thāne, Maharashtra, India beBeeStatistical Full time ₹ 17,40,000 - ₹ 24,65,000
Senior Statistical Programmer Job Description

Sponsor-dedicated statistical programmers collaborate with global pharmaceutical clients to drive the next generation of patient treatment.

Position Overview:

Leverage advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead Phase I-IV clinical trials.

Our Values:
  • Apply scientific rigor to reveal data's full promise.
  • Nurture intellectual curiosity and encourage new challenges with enthusiasm and discovery.
  • Believe in collaboration, diversity of perspectives, and innovative solutions using leading-edge technology.
Responsibilities:
  • Manipulate, analyze, and report clinical trial data using SAS programming.
  • Generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and figures.
  • Produce and QC/validation programming.
  • Generate complex ad-hoc reports utilizing raw data.
  • Perform efficacy analysis.
  • Submit documents and eCRTs.
  • Communicate with internal teams and clients for project specifications, status, issues, or inquiries.
  • Lead duties when called upon.
  • Collaborate as a team player, adaptable, and flexible.
Qualifications:
  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience with clinical trial data in Pharmaceutical & Biotech industry.
  • Study lead experience, preferably juggling multiple projects simultaneously.
  • Strong SAS data manipulation, analysis, and reporting skills.
  • CDISC SDTM / ADaM standards.
  • QC/validation skills.
  • Ad-hoc reporting skills.
  • Efficacy analysis.
  • Drug development life cycle and clinical trials' data manipulation, analysis, and reporting experience.
  • Submissions experience.

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