Senior Data Analyst

4 days ago

Alwar, Rajasthan, India beBeeStatistical Full time ₹ 24,00,000 - ₹ 28,00,000

Sponsor-dedicated: A Critical Role in Innovation

As a Senior Statistical Programmer, you will be at the heart of our client's innovation team, working closely with a global pharmaceutical client to drive the next generation of patient treatment.

Position Overview:

This exciting opportunity involves leveraging advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. The role can be performed fully remotely.

Our Values:
  • We apply scientific rigor to unlock the full promise inherent in data.
  • We foster intellectual curiosity and encourage new challenges with enthusiasm and discovery.
  • We value collaboration and invite diverse perspectives to create possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities:

  • Perform data manipulation, analysis, and reporting for clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming.
  • Generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
  • Produce and quality check/validation programming.
  • Generate complex ad-hoc reports using raw data.
  • Apply strong understanding/experience of Efficacy analysis.
  • Create and review submission documents and eCRTs.
  • Communicate with internal cross-functional teams and clients for project specifications, status, issues, or inquiries.
  • Perform lead duties when called upon.
  • Serve as a team player, willing to go the extra distance to get results, meet deadlines, etc.
  • Be adaptable and flexible when priorities change.

Qualifications:

  • 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, 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 manipulating, analyzing, and reporting clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.
  • Experience supporting immunology, respiratory, or oncology studies would be beneficial.
  • Excellent analytical and troubleshooting skills.
  • Ability to provide high-quality output and deliverables within challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

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