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Biostatistician with SAS Programming (Clinical) Location: US-NJ-Bridgewater Township Jobcode: ea1cdd8942bc055684188f7547b163a3-122020 Email Job
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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. 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. Lead and perform statistical analyses,
modeling, reporting, analytic interpretations, and slide development.
Develop SAS macro libraries to standardize disease identification,
cohort constructions, mapping of healthcare resource utilization and
expenditures to standard metrics for product value propositions.
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. Establish
and main variety of disease identification and composite comorbidity
assessment tools and algorithms. Conduct analytic quality assurance
procedures. Provide timely analytic support for abstract and
manuscript development and submissions to medical/scientific
congresses or publications. Provide analytic support for internal and
external communications and statistical interpretations of data under
the guidance of departmental methodological principles. 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.
Provide 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.
Years of Experience: 6 - 9 Years
madagoni LLC
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