Senior Data Analyst

2 days ago


India beBeeStatistical Full time US$ 90,000 - US$ 1,20,000

Job Overview:

We are seeking a skilled Statistical Programmer to join our team. In this role, you will be responsible for data manipulation, analysis and reporting of clinical trial data.

  • 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

Key Responsibilities:

  • Support or lead one or more Phase I-IV clinical trials
  • Collaborate with cross-functional teams to deliver project specifications, status, issues or inquiries
  • Communicate effectively with internal and external stakeholders
  • Perform lead duties when called upon
Requirements:
  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry
  • Strong SAS data manipulation, analysis and reporting skills
  • Solid experience implementing the latest CDISC SDTM / ADaM standards
  • Good ad-hoc reporting skills
Benefits:
  • Opportunity to work on exciting projects with global pharmaceutical clients
  • Chance to collaborate with talented professionals from diverse backgrounds
  • Professional growth and development opportunities
Additional Information:
  • Experience supporting immunology, respiratory or oncology studies is a plus
  • Excellent analytical & troubleshooting skills
  • Ability to work effectively and successfully in a globally dispersed team environment


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