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Statistical Programmer III

ArtechInformationSystemLLC

East Hanover, NJ, United States contract

Posted: February 9, 2016

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Quick Summary

A Statistical Programmer III is responsible for analyzing and developing statistical models to support business decision-making and drive growth.

Required Skills

SAS Programming MACROs Database Design Statistical Analysis CDISC Regulatory Requirements Collaboration English Proficiency Problem-Solving HARP

Job Description

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.

Job Description

Min 2-3 years of programming experience in HARP, the GSK programming environment is required.

At least 8 years work experience in a Statistical (SAS) programming role preferably supporting clinical trials or in the pharmaceutical industry (5 years for Masters in Mathematics, Statistics/Computer Science or health science graduates).

Advanced knowledge of / experience with SAS and other relevant programming software.

Proven experience in development of advanced MACROs with high programming efficiency; strong programming and problem-solving skills.

Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent).

Expertise in programming according to specifications of analysis datasets, pooled datasets, listings, tables and figures for clinical trials and submission activities. 

Working knowledge of database design/structures and basic statistics. Working experience in pooling analysis datasets across multiple clinical studies (or equivalent).

Good understanding of global clinical trial/project practices, procedures, methodologies.

Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).

Oncology experience preferred

Strong expertise in CDISC on the submission bucket including CRT programming will be a definite plus.

Intermediate knowledge of office tools

Fluent English (oral and written)

Excellent in people interaction and be a collaborative team player.

Education:

Must have a BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s).

Richha Saini

Senior Clinical/Scientific Recruiter

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 

Office: 973.967.3439 | Fax: 973.998.2599

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