Statistical Programmer Consultant

Tandym Group Internal; Novato (CA); Remote; USD 80,000 - 120,000; Full time

Job summary

A leading Life Sciences Company seeks a Statistical Programmer for a remote 6-month contract. The role involves programming responsibilities, dataset creation, and collaboration with various departments to ensure timely project deliverables. Ideal candidates will possess a Master's Degree and relevant programming experience in the clinical trial field.

Qualifications

• Master's Degree in relevant field is required.
• 1-5 years of clinical trial programming experience is preferred.
• Knowledge in SDTM, ADaM, and other statistical software is essential.

Responsibilities

• Provides support on all statistical programming matters according to project strategy.
• Involved in programming activities across various projects and therapeutic areas.
• Works collaboratively with clinical operations and project management to meet deliverables.

Skills

Advanced SAS programming skills

Experience in R

CDISC knowledge

Excellent organizational skills

Ability to prioritize tasks

Education

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

Job description

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