Biostatistician with SAS Programming I (20-00044) – NJ – Bridgewater

Duties:           
To perform tasks under the guidance of project lead or 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 dept.
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 dept. initiatives
Provides consultation for all dept. 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: 0 to 3 years.
 
Skills:
Proficient with SAS or R
Have experience working on Phase 2, 3 or 4 clinical trials
 
Education:    
Master or PhD in statistics or biostatistics
Source: Job Diva – Job Listing

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