Clinical Data Analyst Specialist

6 days ago

Nellore, Andhra Pradesh, India beBeeData Full time ₹ 15,00,000 - ₹ 20,00,000

Imagine working at the heart of innovation in patient treatment, where individuals are empowered to work with autonomy and ownership.

This is an exciting time to be part of our new program 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.

This role can be performed as fully remote, allowing you the flexibility to work from anywhere while still being part of a collaborative team environment with cross-cultural partners.

Job Overview:
  • 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
  • Perform lead duties when called upon
  • Serve as a team player, willing to go the extra distance to get results, meet deadlines, etc.

Responsibilities Summary:

The ideal candidate will have a bachelor's degree in Statistics, Computer Science, Mathematics, or related field, and at least 7 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry.

Additional qualifications include strong SAS data manipulation, analysis, and reporting skills, solid experience implementing CDISC SDTM / ADaM standards, good ad-hoc reporting skills, and proficiency in Efficacy analysis.

Qualifications:

  • 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 CDISC SDTM / ADaM standards
  • Good ad-hoc reporting skills
  • Proficiency in Efficacy analysis

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