Data Driven Clinical Trials Specialist

5 days ago


Tiruchi, Tamil Nadu, India beBeeStatistical Full time ₹ 80,00,000 - ₹ 1,50,00,000

Job Description

We are seeking a skilled Senior Statistical Programmer to join our team. In this role, you will be working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you.

You will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials.

This role can be performed as fully remote, and we are looking for someone who is adaptable and flexible when priorities change.

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.
  • Efficacy analysis.
  • Submission documents and eCRTs.
  • Internal cross-functional teams and client for project specifications, status, issues, or inquiries.

Requirements

  • Bachelor's degree in 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.
  • Study lead experience, preferably juggling multiple projects simultaneously.
  • SAS data manipulation, analysis, and reporting skills.
  • CDISC SDTM/ADaM standards.
  • QC/validation skills.
  • Ad-hoc reporting skills.
  • Efficacy analysis.
  • Familiarity with drug development life cycle.


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