Advanced Statistical Programmer

5 days ago

Anantapur, Andhra Pradesh, India beBeeStatistical Full time ₹ 1,20,00,000 - ₹ 1,50,00,000
Senior Statistical Programmer

Job Description:

The successful candidate will have the opportunity to work with a global pharmaceutical client, driving the next generation of patient treatment. As a Senior Statistical Programmer, 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.

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 internal cross-functional teams and clients for project specifications, status, issues, or inquiries.
  • Lead duties when called upon.
  • Serving as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
  • Being adaptable and flexible when priorities change.

Qualifications:

  • 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.
  • Experience supporting immunology, respiratory, or oncology studies would be a plus.
  • Excellent analytical and troubleshooting skills.
  • Ability to provide quality output and deliverables, in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Benefits:

Our company is committed to providing consistent training, development, and support to enable employee success. We value intellectual curiosity, collaboration, innovation, and adaptability. If you are a motivated and detail-oriented individual with a passion for statistical programming, we encourage you to apply for this exciting opportunity.

Others:

This is an excellent opportunity to grow professionally while making a meaningful impact in the pharmaceutical industry. We look forward to receiving your application

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