Biostatistical Programming Mgr

Amgen Inc

Hyderabad, India
6+ years statistical programming experience
Sas and cdisc sdtm/adam standards expertise
Study lead programmer responsibilities
The role involves leading one or more studies end-to-end as a Study Lead Programmer while managing a team of statistical programmers

Job Summary

  • The role involves leading one or more studies end-to-end as a Study Lead Programmer while managing a team of statistical programmers.
  • Candidates must possess deep expertise in clinical trial operations, SAS programming, and CDISC standards including SDTM and ADaM.
  • Amgen offers vast opportunities for professional growth within a diverse and inclusive global organization committed to patient care.

Matching Summary

The role involves leading one or more studies end-to-end as a Study Lead Programmer while managing a team of statistical programmers.

Skills & Requirements

Must-have

  • 6+ years statistical programming experience
  • SAS and CDISC SDTM/ADaM standards expertise
  • Study Lead Programmer responsibilities
  • Team leadership and management skills
  • Clinical trial process knowledge

Nice-to-have

  • Experience with R or Python tools
  • Regulatory submission experience
  • Automation platform familiarity
  • Global team collaboration ability

Key Requirements

  • BA/BSc degree in quantitative field
  • Minimum 6 years clinical development experience
  • Proven track record leading programming teams
  • Advanced SAS and regulatory compliance skills

Work Rights

Not specified

Tailored Resume

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