Associate SAS Programmer
The Emmes Corporation, established in 1977, is a privately-owned Contract Research Organization (CRO). Headquartered in Rockville, Maryland Emmes employs over six hundred staff worldwide with offices located in Frederick, Maryland, Vancouver, Canada and Bangalore, India. Ranked as a top area workplace of choice by the Washington Post, Emmes fosters an environment of collaboration, professional growth, and exceptional work life balance.Our studies impact public health initiatives on a global scale occurring in more than sixty countries spanning across six continents. We are dedicated to providing statistical and epidemiological expertise, computer systems deployment, data management, study monitoring, regulatory guidance, and overall operational support to clients engaged in biomedical research. Emmes offers support for the entire process of clinical trials from study design and protocol development through data analysis and manuscript generation.
Primary PurposeThe Associate SAS Programmer collaborates with statisticians and data management staff to provide programming support for clinical research studies. As part of these activities, the Associate SAS Programmer produces tables, figures, and listings for clinical study reports, interim reports, ad-hoc reports, and manuscripts. Additional duties also include production of complex HTML reports to summarize accruing data on study websites. The Associate SAS Programmer produces and ensures compliance with CDISC standard datasets such as SDTM and ADaM and develops, maintains, and improves company-specific standard SAS programs. Responsibilities
Provide statistical programming support for multiple clinical research projects
Produce datasets, analyses, tabulations, graphics and listings of clinical trials data
Contribute to on-going quality improvement efforts within the project
Bachelor’s degree, scientific discipline preferred
SAS Certified Base Programmer certification required
Experience in the production of datasets, analyses, tabulations, graphics and listings from clinical trial data
Familiarity with Version 9 (preferably at least 9.3): Base SAS, SAS/STAT, SAS Macro language and SAS SQL; SAS/GRAPH a plus
Experience with development, documentation, and testing of analysis data and programming code to meet regulatory and company standards
Good organizational and communication skills, the ability to work in a collaborative environment, and a desire to improve skills are essential
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The EMMES Corporation is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.