Biostatistical Programming Senior Associate

Amgen Inc

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

Job Summary

  • This role involves performing hands-on statistical programming activities to support complex clinical study data analysis and regulatory submissions.
  • Candidates will create and validate complex SDTM, ADaM datasets, and safety/efficacy tables, listings, and figures using SAS or R.
  • The position offers opportunities for professional growth within a diverse global team dedicated to serving patients through biotechnology innovation.

Matching Summary

This role involves performing hands-on statistical programming activities to support complex clinical study 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 programming expertise
  • CDISC SDTM and ADaM standards knowledge
  • Clinical trial data manipulation skills
  • Complex tables listings figures validation

Nice-to-have

  • Experience with open-source tools like Python
  • Prior regulatory submission experience
  • Automation platform familiarity
  • Global cross-cultural collaboration skills
  • Backup Study Lead Programmer capability

Key Requirements

  • BA/BSc degree in quantitative field
  • Minimum 4 years clinical programming experience
  • In-depth knowledge of SAS/STAT packages
  • Strong English communication skills

Work Rights

Not specified

Tailored Resume

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