Data Analyst and Statistician

3 days ago

Ahmedabad, Gujarat, India beBeeStatistical Full time ₹ 1,44,00,000 - ₹ 1,92,00,000

Job Description

We are seeking a highly skilled Senior Statistical Programmer to join our team. As a Senior Statistical Programmer, you will be dedicated to working with one of our global pharmaceutical clients, driving the next generation of patient treatment. You will be responsible for leveraging 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 is an exciting opportunity to work at the heart of our client's innovation. You will have the autonomy to work independently, collaborating with cross-functional teams and clients to ensure project specifications, status, issues or inquiries are met.

Key Responsibilities:

  • Performing 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

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.

Benefits

  • Consistent training, development and support to enable success
  • A globally dispersed team environment with cross-cultural partners
  • The ability to provide quality output and deliverables, in adherence with challenging timelines

About Us

We are committed to nurturing intellectual curiosity and encouraging everyone to approach new challenges with enthusiasm and the desire for discovery.

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