Statistical Programmer Consultant

Tandym Group; United States; Remote; USD 150,000 - 160,000; Full time

Job summary

A leading Life Sciences Company is seeking a Statistical Programmer to provide essential programming support for clinical studies. This 6-month remote contract focuses on SDTM/ADaM programming and requires strong SAS skills and a Master's degree. Ideal candidates will have 1-5 years of relevant experience and excellent prioritization skills.

Qualifications

• 1-5 years of clinical trial programming experience in the biotechnology/health industry.
• In-depth knowledge in CDISC including SDTM, ADaM, controlled terminologies.

Responsibilities

• Provides programming support for Phase 1 to 3 studies.
• Programs SDTM/ADaM/TLFs for studies, identifies changes in project requirements.
• Works collaboratively with various teams to meet project deliverables.

Skills

Advanced SAS programming

Organizational skills

Prioritization

Education

Master's Degree in Statistics, Computer Science, Mathematics, Engineering

Tools

R

S-Plus

Job description

This range is provided by Tandym Group. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$73.00/hr - $73.00/hr

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

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Information Technology

• Industries

  Technology, Information and Internet

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