Principal Clinical Programmer (dm Sas)

Syneos Health

6+ years dm sas clinical programming experience
Sas listings and macro creation
Data imports and acquisition
The role serves as a lead Clinical Programmer responsible for managing project timelines and delivering software solutions for drug development

Job Summary

  • The role serves as a lead Clinical Programmer responsible for managing project timelines and delivering software solutions for drug development.
  • Candidates will utilize tools like Medidata Rave, Oracle Inform, and SAS to design, validate, and maintain clinical data applications.
  • Syneos Health offers a supportive culture with career development opportunities and a commitment to building an inclusive workplace.

Matching Summary

The role serves as a lead Clinical Programmer responsible for managing project timelines and delivering software solutions for drug development.

Skills & Requirements

Must-have

  • 6+ years DM SAS Clinical Programming experience
  • SAS listings and macro creation
  • Data imports and acquisition
  • Study build and SAS mapping
  • Electronic Data Capture (EDC) support

Nice-to-have

  • Experience in matrix-structured environment
  • Strong communication and interpersonal skills
  • Ability to manage multiple concurrent studies
  • Leadership and training of junior programmers
  • Proficiency in PL/SQL or C#

Key Requirements

  • Bachelor's degree preferred
  • Base and Advanced SAS certification preferred
  • Minimum 6 years of DM SAS experience
  • Oversight experience for 4-5 studies
  • Ability to travel up to 25%

Work Rights

Not specified

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