Biostatistical Programming Senior Associate

Amgen UK

Hyderabad, India
Not specified; not specified; generous total rewar...
4 years statistical programming experience
Sas and/or r proficiency
Cdisc sdtm and adam standards knowledge
This role involves performing hands-on statistical programming to support complex clinical trial data analysis and regulatory submissions

Job Summary

  • This role involves performing hands-on statistical programming to support complex clinical trial data analysis and regulatory submissions.
  • The position requires creating and validating complex SDTM, ADaM datasets, tables, listings, and figures for both safety and efficacy.
  • Amgen offers vast opportunities to learn and move up within a diverse and inclusive global organization.

Matching Summary

This role involves performing hands-on statistical programming to support complex clinical trial data analysis and regulatory submissions.

Salary

Not specified; Not specified; Generous Total Rewards Plan comprising health, finance, work/life balance, and career benefits

Skills & Requirements

Must-have

  • 4 years statistical programming experience
  • SAS and/or R proficiency
  • CDISC SDTM and ADaM standards knowledge

Nice-to-have

  • Experience with R and Python automation
  • Prior regulatory submission experience
  • Global cross-cultural collaboration skills

Key Requirements

  • BA/BSc or higher degree in quantitative field
  • Minimum 4 years of clinical statistical programming experience
  • In-depth knowledge of SAS/STAT packages

Work Rights

Not specified

Tailored Resume

Cover Letter