SAS Programmer - MacroGenics (Rockville, MD)

MacroGenics, Inc., a growing biotechnology company, has an opening for a SAS Programmer at its office in Rockville, MD. Together with biostatisticians, clinicians and development personnel, this individual will work on a number of high-impact clinical and epidemiological study projects. This is a unique opportunity to make a valued contribution on drug development efforts. Responsibilities include developing, modifying, and maintaining an integrated and reusable programming suite, primarily in SAS, in support of biostatisticians and clinical team across multiple projects concurrently; understanding the reporting and data cleaning needs for clinical studies, and creating suitable representative data presentations; designing and developing project-specific SAS programs for biostatisticians, often producing analysis datasets; development of utilities for QC/QA and analyses; develops listings and integrated computer programs to assist in the data review process and to provide operational metrics on resources and timelines; assist in the design and creation of a cohesive, integrated programming environment capable of responding quickly to changing needs and being regulatory compliant; assist in building an integrated infrastructure for a growing company; assist in data retrieval from Oracle Clinical, vendors and other sources; participates in all study team meetings providing a single point of contact for all SAS programming related activities and deliverables; recommend and participate in overall process improvements for programming; assists in the development of guidelines and workflows for programming activities; assists with other departmental tasks and responsibilities as needed.

Qualifications

Applicants must meet the following requirements: A minimum of 6 years experience in SAS Programming, with 3 years experience in drug development, biostatistics background and supervisory experience is a plus; Bachelors degree in Computer Sciences, Statistics, Mathematics or relevant scientific discipline; proven success in the development, documentation and qualification of programs to generate Tables, Listings and Figures for Clinical Studies; demonstrated experience in base SAS, SAS MACRO, SQL, and using ODS for presentations and data mining reports; strong quantitative and analytical skills, with the ability to identify problems in complex algorithms and provide working solutions; must have a high level of attention to detail; demonstrated knowledge and understanding of programming standards and methodologies, GCP, ICH and related FDA regulations; experience with the CDISC standard is a plus; ability to manage and prioritize multiple tasks concurrently; experience with Oracle Clinical, Integrated Review, or other relational data management software is considered a plus; experience with EDC data and products is a plus.

Send resume and salary requirements to 1500 East Gude Drive, Rockville, MD 20850, email to HResources@macrogenics.com, or fax to (301) 251-5321. Reference Job Code # 08008 in all correspondence. Visit www.macrogenics.com for more details.

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