Data Driven Innovator

2 days ago

Malappuram, Kerala, India beBeeStatisticalProgrammer Full time ₹ 1,50,00,000 - ₹ 2,00,00,000

About This Role:

As a senior statistical programmer, you will be embedded within a global pharmaceutical client, driving innovation and empowering individuals to work with autonomy and ownership.

This is an exciting time to be part of this new program, where you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead Phase I-IV clinical trials.

Cytel values collaboration, diversity, and innovation. Our team believes in applying scientific rigor, nurturing intellectual curiosity, and seeking intelligent solutions using leading-edge technology.

  • We apply scientific rigor to reveal the full promise inherent in data.
  • We nurture intellectual curiosity and encourage enthusiasm for discovery.
  • We collaborate and invite diverse perspectives to create possibilities.
  • We prize innovation and seek intelligent solutions.

Main Responsibilities Include:

  • Data manipulation, analysis, and reporting of clinical trial data, utilizing SAS programming.
  • Generating and validating SDTM and ADaM datasets/analysis files, tables, listings, and figures.
  • 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 cross-functional teams and clients for project specifications, status, issues, or inquiries.
  • Performing lead duties when called upon.
  • Being adaptable and flexible when priorities change.

Qualifications and Requirements:

  • Bachelor's degree in Statistics, Computer Science, Mathematics, or related field.
  • At least 7 years of SAS programming experience working with clinical trial data in 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.
  • Good ad-hoc reporting skills.
  • Proficiency in Efficacy analysis.
  • Familiarity with drug development life cycle and clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.

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