New job Biostatistician with SAS programming skills – 1 year contract (New Jersey)

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Group: Job Openings, Job Leads and Job Connections! Subject: Biostatistician with SAS programming skills – 1 year contract (New Jersey) Margaret Imperiale posted a job: Biostatistician with SAS programming skills – 1 year contract (New Jersey) "To view this and other current positions please visit www.JGBBioPharma.com. Interested parties should contact Nicole@JGBBioPharma.com. *Current U.S. work permit status required. No VISA sponsorship provided* DESCRIPTION: To perform tasks under the guidance of project lead or GEVD departmental principals on analytic design and statistical analytic planning, coordinate real world database management, and data warehouse construction or maintenance; to develop documentations of analytic plans, prepare for statistical concept communications and be able to advise on analytic strategies and recommend methodological solutions on complex analytic topics; to lead and perform statistical analysis, modeling, reporting, analytic interpretations, and slide development; to develop SAS macro libraries to standardize disease identification, cohort constructions, mapping of healthcare resource utilization and expenditures to standard metrics for product value propositions; to construct drug coding systems to support database activities for key therapeutic R&D and brand LCM activities, and establish and maintain a repository of the coding systems for therapeutic medications, diagnostic or surgical procedures and drug delivery systems ; to establish and main variety of disease identification and composite comorbidity assessment tools and algorithms; to conduct analytic quality assurance procedures; to provide timely analytic support for abstract and manuscript development and submissions to medical/scientific congresses or publications; to provide analytic support for internal and external communications and statistical interpretations of data under the guidance of departmental methodological principals. Roles & Responsibilities: • Develop statistical analytic plans, statistical expertise and data management techniques and skills • Manage real world database operations, analytic programming and statistical modeling activities • Assist project lead or departmental principals in study design, power calculation, CRF construction, analytic operations and reporting for retrospective and prospective studies • Assist project lead or departmental principals in analytic/computing resource planning,, work flow management and prioritization, and related logistic coordination • Prepare communication materials on analytic projects including processes, data, analytic findings for internal and external functional groups within or outside of GEVD • Prepare slide decks for congress or manuscript submissions or internal or external communications • Plan and initiate analytic projects using the real world databases or clinical trial data warehouse in support of the GEVD initiatives • Provides consultation for all GEVD groups on research methodology and statistical or analytic issues • Vendor Management • Database licensing and maintenance • Analytic process formulation and standardization • Potentially supervising team of analytic and programming support EXPERIENCE AND QUALIFICATIONS: • Working knowledge of healthcare industry • Strong expertise in SAS programming and other related analytic software and power estimation • Solid knowledge in experimental design and observational study methodology • Ability to perform statistical, analytic and programming tasks with high efficiency and limited guidance • Be willing and able to work flexibly • PhD in statistics, econometrics, psychometrics, or related quantitative sciences, or master’s degree in statistics plus >10 years of experiences in claims database analytic work and statistical modeling Margaret Imperiale, Administrative Services www.JGBBioPharma.com"

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