Highly Skilled Statistical Analyst

7 days ago


Bharatpur, Rajasthan, India beBeeStatistical Full time ₹ 20,00,000 - ₹ 24,00,000

Sponsor-dedicated:

You will be embedded within a global pharmaceutical client, working closely with their team to drive innovation. As a Senior Statistical Programmer, you will be dedicated to one of our clients who is leading the way in patient treatment. This is an exciting time to be part of this new program.

**Job Overview:**

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.

Our Values

  • We apply scientific rigor to reveal the full promise in data.
  • We nurture intellectual curiosity and encourage enthusiasm for discovery.
  • We believe in collaboration and invite diverse perspectives to create possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities

You will contribute by:

  1. Performing data manipulation, analysis and reporting of clinical trial data, utilizing SAS programming.
  2. Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures.
  3. Producing and QC / validation programming.
  4. Generating complex ad-hoc reports utilizing raw data.
  5. Applying strong understanding/experience of Efficacy analysis.
  6. Creating and reviewing submission documents and eCRTs.
  7. Communicating with internal cross-functional teams and clients for project specifications, status, issues or inquiries.
  8. Performing lead duties when called upon.
  9. Serving as a team player, with a willingness to go the extra distance to get results.

Qualifications

To succeed in this position, you will have:

  • A Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience 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.
  • 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.


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