Biostatistician with SAS Programming II (4533692)

Artech Information System LLC; Swiftwater (Monroe County); On-site; USD 90,000 - 125,000; Full time

Job summary

A leading IT staffing company in the United States is seeking a skilled Biostatistician. The role involves providing statistical expertise for clinical trial data analysis and supporting multidisciplinary teams. Responsibilities include managing statistical tasks, contributing to study documentation, and ensuring data quality in compliance with regulatory standards. Ideal candidates will have 3-6 years of relevant experience and strong knowledge of SAS programming.

Qualifications

• 3-6 years of relevant experience in biostatistics.
• Experience in managing tasks at the trial level.
• Knowledge of SAS programming.
• Ability to support Phase I–III studies.

Responsibilities

• Provide statistical support to other statisticians.
• Produce synopsis and statistical sections of the protocol.
• Participate in programming activities for studies.
• Review and approve study-related documents.
• Compute sample sizes and discuss trial design.
• Compute sample sizes, discuss trial design, and create randomization."
• Collaborate with programmers to ensure statistical programs are developed, tested, and validated before analysis date.

Skills

Statistical Analysis

Knowledge of SAS programming

Ability to support Phase I - III studies

Ability to work on multiple studies

Tools

SAS tools

Job description

Biostatistician with SAS Programming II (4533692)

Contract

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

This individual will provide statistical expertise to support the research and development of our products. He/she will provide critical input on the design and analysis of our clinical trial data so that accurate assessments are made for decision‑making.

This individual will have to use his/her technical expertise to make the appropriate decision concerning which method to use for analyzing data. He/she will also have to provide a critical review to ensure the correctness of results for accurate decision‑making. He/she will have to work in a multidisciplinary team and will have to effectively communicate to team members who may not have the same training.

We operate in a highly regulated environment; therefore, we must ensure that our work is of the highest quality and will withstand the scrutiny of regulatory agencies around the world. This individual must possess the ability to work on several different projects that are at different stages while managing the details is highly important.

Responsibilities

• Provide statistical support to other statisticians through the management of tasks at the trial level
• With supervision by a more senior statistician or head of Biostatistics, produce synopsis, statistical section of the protocol, and SAP for specific studies
• Participate in programming activities (analysis files, TLFs, randomization, ...)
• With supervision by a more senior statistician or head of Biostatistics, complete the statistical section of the iCSR
• Review and approve study-related documents (CRFs, DEPs, ...)
• With supervision by a more senior statistician or head of Biostatistics, compute sample sizes, discuss trial design, and create randomization
• In collaboration with the programmers, ensure that statistical programs are developed, tested and validated prior to the target analysis date.

Skills

• 3-6 years of relevant experience
• Statistical Analysis
• Knowledge of SAS programming
• Ability to support Phase I - III studies (mainly phase II/III)
• Ability to work on multiple studies at one time