Statistical Programmer Consultant

  • Novato, CA
  • Posted 2 days ago | Updated 1 hour ago

Overview

On Site
$73 - $73 per hour
Contract - W2
Contract - 6 month(s)

Skills

Statistical Programmer Consultant

Job Details



Our client, a leading Life Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring project work.


This is a 6-month contract, 100% REMOTE.


**Qualified candidates must be able to work on a W2 basis.


Responsibilities:



  • Provides timely support to the project team on all statistical programming matters according to the project strategy.

  • Programs SDTM/ADaM/TLFs for the studies, write datasets specification, QC datasets and tables. Identifies and communicates changes in project requirements that may affect key deliverables.

  • Involved in the programming activities on multiple projects/ studies across various therapeutic areas, both internally and externally by CROs

  • Creates and reviews annotated CRF to SDTM datasets

  • Provides support in balancing conflicting priorities, promoting communication and adequate information flow to motivate, encourage and align people with the company' s strategic objectives

  • Functions as a positive role model for setting high expectations for quality, creativity and project ownership

  • Works collaboratively with Clinical Operations, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting

  • Provides technical input into documents produced by other functions (e.g., biostatisticians, data managers, medical writers)

  • Works with Biometrics and other functions for the development and maintenance of the data review and reporting tools, and any other statistical applications as appropriate


Qualifications:



  • Master's Degree in Statistics, Computer Science, Mathematics, Engineering or related discipline

  • Minimum of 1-5 years of clinical trial programming experience in the biotechnology, pharmaceutical or health related industry

  • Advanced SAS programming skill s and experience in other statistical software, such as R and S-Plus

  • Experience and in-depth knowledge in CDISC including SDTM, ADaM, and controlled terminologies

  • Excellent organizational skills and ability to prioritize tasks


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