Biostatistician with SAS Programming III (20-00060) – NJ – Bridgewater

Duties:
To perform tasks under the guidance of project lead or CMS 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.
 
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 CMS � 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 CMS initiatives � Provides consultation for all CMS 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.  

Skills: 
Good knowledge of pharmaceutical clinical development, together with Late Phase experience.
Demonstrated strong interpersonal and communication skills

Education: 
PhD/MS in statistics or related discipline with at least 6 years of pharmaceutical experience
 
Source: Job Diva – Job Listing

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