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HomeCompaniesIblyjb Fa Ocs Oraclecloud Com CX 2001Principal Statistical Programmer FSP - RWD/EPI

Principal Statistical Programmer FSP - RWD/EPI

Iblyjb Fa Ocs Oraclecloud Com CX 2001 · United States; United States - Remote - Eastern Time, Cambridge, MA, US; Canada - Remote - Eastern Time, Toronto, ON, CA · Remote · Deleted · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyIblyjb Fa Ocs Oraclecloud Com CX 2001
TitlePrincipal Statistical Programmer FSP - RWD/EPI
Normalized title-
Department / teamStatistical Programming - FSP
LocationUnited States
Work modelRemote / Remote
Employment typeFull Time
Salary-
Statusdeleted
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-04-02 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-03

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Department jobsActive postings in Statistical Programming - FSP.Open
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Linked records

CompanyIblyjb Fa Ocs Oraclecloud Com CX 2001
Source118dd8bd-c51f-43c2-93a6-817304220200
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description You will contribute by: Providing support to the Epidemiology team by preparing Real World data, advising on data analytic strategies, and supporting stakeholders in various epidemiology analytic activities Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of statistical packages or platforms Supporting statistical programming to generate innovative means of data standardization, visualization, and reporting of observational data Supporting Medical Affairs (e.g. observational studies leveraging RWD); Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the development of regulatory/safety documents, and Clinical Development (e.g.; assessment of patient populations/ protocol feasibility) The position will partner with Epidemiologists to manage relationships with internal and external stakeholders Being able to prioritize and manage work across multiple projects and stakeholders Providing strong communication to ensure successful and timely project delivery Solving technical problems with experience and expertise Responsibilities Summary of Key Responsibilities: Assist in development of study protocols and analysis plans leveraging large RWD sources (Claims and/or EHR) Liaise with data vendors to obtain relevant data extracts for research studies consistent with study protocols Create analytical databases from data extracts to facilitate conduct of data analyses Conduct analyses consistent with methods set forth in study protocols and analysis plans Produce tables and figures for discussions with other investigators, clients, and for study reports Present results internally and to clients Assist in the preparation of study reports and other deliverables May have supervisory responsibilities in the future Qualifications What we’re looking for: Master’s degree or PhD in related field (epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution Intermediate to expert level proficiency in SQL is a must. In addition, SAS or R proficiency is required Deep expertise analyzing RWE data sources such as Optum (Clinformatics Datamart® and Market Clarity), Truveta and UK Biobank. Experience analyzing clinical trial and/or registry data is desirable Familiarity with relational databases and proficient understanding of claims and ancillary file layouts Experience with applied statistics including regression analysis (OLS, longitudinal, logistic, Cox, GLM/GEE), survival analyses (Kaplan-Meier, cumulative incidence, accelerated failure time models), and propensity weighting Excellent project management skills; can prioritize multiple tasks and goals to ensure timely completion Confident and competent when interacting with internal and external stakeholders Strong written/verbal communication skills. Highly effective at summarizing and presenting key considerations and evidence

Full job record

Job ID3b4bfaa0c0bea1c94ed1d65e776f56b6858602f5
Org ID1db7e607-b344-4109-abb0-4cfac49e25b6
Source ID118dd8bd-c51f-43c2-93a6-817304220200
Board ID118dd8bd-c51f-43c2-93a6-817304220200
Provideroracle_hcm
Provider Job Key1414
TitlePrincipal Statistical Programmer FSP - RWD/EPI
Normalized Title
Statusdeleted
Activeno
Location TextUnited States; United States - Remote - Eastern Time, Cambridge, MA, US; Canada - Remote - Eastern Time, Toronto, ON, CA
DepartmentStatistical Programming - FSP
Team
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryUnited States
Region
City
Salary RawDescription You will contribute by: Providing support to the Epidemiology team by preparing Real World data, advising on data analytic strategies, and supporting stakeholders in various epidemiology analytic activities Programming and conducting statistical analysis under the direction and supervision of epidemiologists/statisticians including data coding, creation of algorithms, linkage of datasets, and use of statistical packages or platforms Supporting statistical programming to generate innovative means of data standardization, visualization, and reporting of observational data Supporting Medical Affairs (e.g. observational studies leveraging RWD); Global Patient Safety and Risk Management (e.g., analysis to obtain background rates) for the development of regulatory/safety documents, and Clinical Development (e.g.; assessment of patient populations/ protocol feasibility) The position will partner with Epidemiologists to manage relationships with internal and external stakeholders Being able to prioritize and manage work across multiple projects and stakeholders Providing strong communication to ensure successful and timely project delivery Solving technical problems with experience and expertise Responsibilities Summary of Key Responsibilities: Assist in development of study protocols and analysis plans leveraging large RWD sources (Claims and/or EHR) Liaise with data vendors to obtain relevant data extracts for research studies consistent with study protocols Create analytical databases from data extracts to facilitate conduct of data analyses Conduct analyses consistent with methods set forth in study protocols and analysis plans Produce tables and figures for discussions with other investigators, clients, and for study reports Present results internally and to clients Assist in the preparation of study reports and other deliverables May have supervisory responsibilities in the future Qualifications What we’re looking for: Master’s degree or PhD in related field (epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution Intermediate to expert level proficiency in SQL is a must. In addition, SAS or R proficiency is required Deep expertise analyzing RWE data sources such as Optum (Clinformatics Datamart® and Market Clarity), Truveta and UK Biobank. Experience analyzing clinical trial and/or registry data is desirable Familiarity with relational databases and proficient understanding of claims and ancillary file layouts Experience with applied statistics including regression analysis (OLS, longitudinal, logistic, Cox, GLM/GEE), survival analyses (Kaplan-Meier, cumulative incidence, accelerated failure time models), and propensity weighting Excellent project management skills; can prioritize multiple tasks and goals to ensure timely completion Confident and competent when interacting with internal and external stakeholders Strong written/verbal communication skills. Highly effective at summarizing and presenting key considerations and evidence
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://iblyjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/1414
Apply URLhttps://iblyjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/1414
First Seen At2026-05-31 17:57:23Z
Last Seen At2026-06-03 10:59:47Z
Last Checked At2026-06-06 11:13:47Z
Last Changed At2026-06-06 11:13:47Z
Inactive At2026-06-06 11:13:47Z
Source Posted At2026-04-02 17:00:31Z
Source Updated At
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=oracle_hcm/board=iblyjb.fa.ocs.oraclecloud.com|CX_2001/date=2026-06-03/2026-06-03T10-59-44-054Z-e920dd32b914250e03c8b11f037cc7dad6e0b094817f34a056d01496b540eb47.json
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