Senior Data Science Expert

4 days ago

Dindigul, Tamil Nadu, India beBeeStatistical Full time ₹ 90,00,000 - ₹ 1,30,00,000

Job Description:

Sponsor-dedicated professionals are sought to work fully embedded within a global pharmaceutical client, with the support of Cytel. You will be at the heart of our client's innovation, driving the next generation of patient treatment.

This is an exciting time to be part of a new program, where individuals are empowered to work with autonomy and ownership. As a senior statistical programmer, 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.

Our team is dedicated to collaboration and invites diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.

Responsibilities:

  • Perform data manipulation, analysis and reporting of 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)
  • Production and QC/validation programming
  • Generate complex ad-hoc reports utilizing 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
  • Lead duties when called upon
  • Be adaptable and flexible when priorities change

Qualifications:

  • 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 the pharmaceutical industry
  • Study lead experience, preferably juggling multiple projects simultaneously preferred
  • Strong SAS data manipulation, analysis and reporting skills
  • Solid experience implementing 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 clinical trials' data
  • Submissions experience using define.xml and other submission documents

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