

Integrated Resources, Inc ( IRI )
RWE Manager
β - Featured Role | Apply direct with Data Freelance Hub
This role is for an RWE Manager, a 12-month freelance position offering competitive pay. Required skills include proficiency in R, Python, or SAS, experience with real-world data, and a Master's or PhD in a relevant field.
π - Country
United States
π± - Currency
$ USD
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π° - Day rate
464
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ποΈ - Date
June 19, 2026
π - Duration
Unknown
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ποΈ - Location
Unknown
-
π - Contract
Unknown
-
π - Security
Unknown
-
π - Location detailed
United States
-
π§ - Skills detailed
#Programming #ML (Machine Learning) #Statistics #Data Science #Monitoring #Python #R #Visualization #Databases #Datasets #AI (Artificial Intelligence) #Data Governance #SAS #Data Privacy #Strategy
Role description
Position Summary
β’ The Real-World Evidence (RWE) team within clientβs Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group.
β’ This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies.
Key Responsibilities
β’ Conduct high-impact research using large-scale observational databases and clinical trial data to generate real-world insights.
β’ Design and execute studies in collaboration with global cross-functional teams, including clinical, regulatory, epidemiology, and data science.
β’ Develop protocols, statistical analysis plans, and programming specifications aligned with international standards.
β’ Deliver high-quality outputs including analysis-ready datasets, visualizations, and manuscripts for peer-reviewed publication.
β’ Present findings to internal and external stakeholders, including global scientific and regulatory audiences.
β’ Stay current with global trends in RWE methodologies, data privacy regulations, and health technology assessment.
Required Qualifications
β’ Masters in Epidemiology, Biostatistics, Data Science, Public Health, Biomedical Informatics, or a related quantitative discipline. Would prefer a PhD with qualifications.
β’ Experience working with real-world data (e.g., electronic health records, claims, registries) from diverse healthcare systems.
β’ Proficiency in R, Python, or SAS; familiarity with OMOP CDM and OHDSI tools is highly desirable.
β’ Strong written and verbal communication skills in English; additional languages are a plus.
β’ Demonstrated ability to work effectively in multicultural, multidisciplinary teams.
Preferred Qualifications
β’ Experience working with data sources from low- and middle-income countries (LMICs), including national health surveys, regional registries, or community-based studies.
β’ Familiarity with LMIC health systems, including data infrastructure, care delivery models, and public health priorities.
β’ Knowledge of global health policies, including WHO guidelines, international data governance frameworks, and health equity initiatives.
β’ Experience with digital health technologies, such as mobile health platforms, remote monitoring tools, or AI-enabled diagnostics.
β’ Prior collaboration with pharmaceutical companies, including experience in clinical development, regulatory strategy, or health economics and outcomes research (HEOR).
β’ Experience with international regulatory submissions or health authority interactions.
β’ Familiarity with machine learning, causal inference, and advanced statistical modeling.
β’ Prior publications in peer-reviewed journals and presentations at global conferences.
Position Summary
β’ The Real-World Evidence (RWE) team within clientβs Innovative Medicine is seeking a highly motivated Postdoctoral Scientist to join our Data Science & Digital Health (DSDH) Immunology group.
β’ This global role offers a unique opportunity to apply advanced analytics to real-world data (RWD) and contribute to the generation of evidence that informs clinical development, regulatory strategy, and healthcare decision-making across diverse populations and geographies.
Key Responsibilities
β’ Conduct high-impact research using large-scale observational databases and clinical trial data to generate real-world insights.
β’ Design and execute studies in collaboration with global cross-functional teams, including clinical, regulatory, epidemiology, and data science.
β’ Develop protocols, statistical analysis plans, and programming specifications aligned with international standards.
β’ Deliver high-quality outputs including analysis-ready datasets, visualizations, and manuscripts for peer-reviewed publication.
β’ Present findings to internal and external stakeholders, including global scientific and regulatory audiences.
β’ Stay current with global trends in RWE methodologies, data privacy regulations, and health technology assessment.
Required Qualifications
β’ Masters in Epidemiology, Biostatistics, Data Science, Public Health, Biomedical Informatics, or a related quantitative discipline. Would prefer a PhD with qualifications.
β’ Experience working with real-world data (e.g., electronic health records, claims, registries) from diverse healthcare systems.
β’ Proficiency in R, Python, or SAS; familiarity with OMOP CDM and OHDSI tools is highly desirable.
β’ Strong written and verbal communication skills in English; additional languages are a plus.
β’ Demonstrated ability to work effectively in multicultural, multidisciplinary teams.
Preferred Qualifications
β’ Experience working with data sources from low- and middle-income countries (LMICs), including national health surveys, regional registries, or community-based studies.
β’ Familiarity with LMIC health systems, including data infrastructure, care delivery models, and public health priorities.
β’ Knowledge of global health policies, including WHO guidelines, international data governance frameworks, and health equity initiatives.
β’ Experience with digital health technologies, such as mobile health platforms, remote monitoring tools, or AI-enabled diagnostics.
β’ Prior collaboration with pharmaceutical companies, including experience in clinical development, regulatory strategy, or health economics and outcomes research (HEOR).
β’ Experience with international regulatory submissions or health authority interactions.
β’ Familiarity with machine learning, causal inference, and advanced statistical modeling.
β’ Prior publications in peer-reviewed journals and presentations at global conferences.






