Contract Statistical Programmer

Cerus; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

An innovative biotechnology firm is seeking a skilled SAS Programmer to join their dynamic team. This remote role involves providing programming support for clinical trials, developing SAS programs, and preparing datasets that adhere to industry standards. The ideal candidate will have extensive experience in SAS programming, a strong understanding of CDISC standards, and the ability to work collaboratively with interdisciplinary teams. If you are passionate about contributing to the advancement of medical research and enhancing patient care, this opportunity is perfect for you.

Qualifications

• 7+ years of SAS programming experience in clinical trials.
• Strong knowledge of Base SAS, SAS/GRAPH, and SAS/STAT.
• Experience with CDISC SDTM and ADaM models.

Responsibilities

• Provide SAS programming support for clinical trials and reports.
• Develop SAS programs to generate TLFs using Base SAS and macros.
• Prepare datasets meeting CDISC SDTM and ADaM standards.

Skills

SAS Programming

Base SAS

SAS Macros

SAS/STAT

SAS/GRAPH

SAS/SQL

CDISC SDTM

ADaM

R

GCP Principles

Education

B.S. in Statistics

M.S. in Biostatistics

Ph.D. in Computer Science

Tools

SAS

R

Job description

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Cerus aims to be the global leader and trusted partner of blood centers and hospitals whose technology, services, and commitment are the lifeblood of safe and accessible blood for patients around the world.

This is a 6-month remote opportunity based out of the US.

Primary Responsibilities:

• Provide SAS programming support for analyzing clinical trials, supporting registrations, and creating reports for publications and ad hoc analyses.
• Develop SAS programs to generate TLFs meeting requirements using Base SAS, SAS Macros, SAS/STAT, SAS/Graph, SAS/SQL within applicable timelines.
• Draft and review data specifications and build analysis datasets.
• Review CRF design, data management plan, data validation plan, and edit check specifications.
• Interact with statisticians and interdisciplinary teams on timelines and content of deliverables.
• Follow validation and verification requirements for software developed within the department, including peer reviews.
• Develop, validate, and maintain macros and tools to enhance efficiency and quality of output.
• Prepare datasets and documentation that meet CDISC SDTM and ADaM standards for submissions.
• Provide technical leadership and support to the Biostatistics department as needed.
• Apply and promote good programming practices.

Qualifications/Requirements/Skills:

• B.S., M.S., or Ph.D. in statistics, biostatistics, computer science, or a related field with at least 7 years of experience as a SAS programmer in clinical trials.
• Excellent knowledge of Base SAS (macro language, Proc SQL, ODS), SAS/GRAPH, and SAS/STAT.
• Good knowledge of CDISC SDTM and ADaM models.
• Experience with ISS/ISE data preferred.
• Experience with other statistical packages (e.g., R, S-plus) is a plus.
• Knowledge of GCP principles and regulatory requirements.
• Aptitude for troubleshooting and independent work.
• Ability to follow validation and data transfer guidelines.
• Strong communication skills and ability to manage workload and priorities.
• Flexible and adaptable to changing priorities.
• Experience running SAS in Windows environment.
• Ability to set realistic timelines and complete tasks accordingly.

All qualified applicants will receive consideration regardless of race, sex, color, religion, sexual orientation, gender identity, national origin, veteran status, or disability.

Additional Details:

• Seniority level: Mid-Senior level
• Employment type: Contract
• Job function: Other and Engineering
• Industries: Biotechnology Research, Medical Equipment Manufacturing, Pharmaceutical Manufacturing