Senior/pr Statistical Programmer

Syneos Health

**
8+ years clinical sas programming experience
Strong adam and tlf programming skills
Experience with sdtm submission packaging
** Syneos Health is seeking a Senior/Pr Statistical Programmer with extensive experience in Clinical SAS programming to support drug development and commercialization efforts. The role involves developing custom programming code, ensuring quality standards, and collaborating with various project team members to drive successful project outcomes. **

Job Summary

  • The role involves using SAS to develop custom code for generating summary tables, listings, graphs, and derived datasets according to statistical analysis plans.
  • As a lead statistical programmer, you will direct the activities of other personnel, review project documentation, and ensure inspection readiness through rigorous quality control.
  • Syneos Health offers a supportive culture focused on career development, technical training, and an inclusive environment where colleagues can authentically be themselves.

Matching Summary

Match Score: 75

** Syneos Health is seeking a Senior/Pr Statistical Programmer with extensive experience in Clinical SAS programming to support drug development and commercialization efforts. The role involves developing custom programming code, ensuring quality standards, and collaborating with various project team members to drive successful project outcomes. **

Skills & Requirements

Must-have

  • 8+ years Clinical SAS Programming experience
  • Strong ADAM and TLF programming skills
  • Experience with SDTM submission packaging
  • Knowledge of DEFINE.xml creation
  • Ability to lead statistical programming teams

Nice-to-have

  • Mentoring new programming associates
  • Participating in industry standards organizations
  • Developing training courses and materials
  • Contributing to standardization macros
  • Active participation in bid defense meetings

Key Requirements

  • Undergraduate degree in scientific or statistical discipline
  • 8+ years of Clinical SAS Programming experience
  • Expertise in safety and efficacy output programming
  • Submission packager creation experience (ADRG, define.xml)

Work Rights

Not specified

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