Statistical Programmer Consultant

Statistical Programmer Consultant

Contract Type:

Contractor

Location:

Novato - CA

Industry:

Life Sciences

Reference Number:

CR/505941

Salary:

$0 - $0 Hourly

Contact Name:

Tandym Group

Contact Email:

titus.wilson@tandymgroup.com

Contact Phone:


Date Published:

05-Jun-2025

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 

Required Experience

  • 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

APPLY NOW

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