Jobs · Information Technology · New Jersey

Clinical Data Scientist/ Methodologist

Sanofi · Bridgewater, NJ · 3 wk ago
HybridInformation TechnologyFull-time

About the role

Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you’ll help advance prevention on a global scale - and shape the future of immunization.

The Data Assessment Center of Excellence (CoE) is a specialized team within Sanofi's Digital RWD & HI function, operating at the intersection of epidemiology, RWD, data products and insights/evidence generation. The vision of the CoE is to ensure all Sanofians have the right data, used the right way, for real patient impact.

Main Responsibilities

  • Lead and execute feasibility assessments for RWD sources (electronic health records, administrative claims, patient registries, wearable/digital health data) to determine suitability for specific research/business objectives
  • Develop and apply structured data assessment frameworks to evaluate data quality dimensions, including accuracy, completeness, validity, timeliness, longitudinally consistency, and integrity
  • Assess the availability and representativeness of patient populations within RWD sources available in Sanofi for both internal decision-making and regulatory-grade evidence generation
  • Evaluate the feasibility of extracting structured and unstructured data elements (e.g., clinical scores, patient-reported outcomes) from EHR systems, including NLP-based extraction from clinical notes
  • Document assessment outcomes in standardized feasibility reports and communicate findings clearly to cross-functional stakeholders
  • Identify and articulate limitations of RWD sources, such as proxy endpoint constraints, population coverage gaps
  • Design methodologically sound recommendations & minimize misuse of RWD, leading to unreliable insights or evidence generation
  • Ensure appropriate use of ICD codes, procedure codes, and other medical coding standards (sourced from peer-reviewed references such as PubMed, Embase, and Orphanet, etc.) for patient identification, healthcare provider segmentation, clinical site identification, and phenotyping
  • Apply advanced epidemiological and biostatistical methods including propensity score methods, time-to-event analyses, sensitivity analyses, and bias assessment
  • Provide methodological input on the use of clinical score proxies and surrogate endpoints in RWD contexts, clearly delineating their applicability for internal versus regulatory/publication use
  • Provide methodology advises ensuring deliverables from RWD Foundation, RWD Science, and RWD Products are based on medical evidence/guidelines, clinically & contextually relevant
  • Work closely with analysts & data scientists to ensure methodological recommendation is realistic and implementable
  • Partner with R&D, Business units (Vaccines, General Medicine and Specialty Care) & Digital teams on data identification and appropriate usage of RWD for insights / evidence generation across drug lifecycle
  • Serve as the methodological point of contact for fit-for-purpose data assessment inquiries from internal stakeholders
  • Collaborate with RWD Foundation, RWD Product Owners, RWD Data Sciences to ensure RWD are used appropriately to inform reliable decision making & to provide knowledge transfer on data domain expertise
  • Manage external data vendors and technology partners (e.g., EHR, claims, registries) to understand data limitations and to verify methodological recommendations when required

About You

  • Advanced degree (Master's or PhD) in Epidemiology, Biostatistics, Health Informatics, Health Economics, Pharmacoepidemiology, or a closely related quantitative discipline
  • Minimum 4-5 years for Master’s degree holder or 2-4 years for Doctoral degree holder of relevant experience in real-world data, commercial analytics, real-world evidence, health outcomes research, fit-for-purpose feasibility assessment, data quality assessment or a related field within the pharmaceutical, biotech, or health technology industry
  • Experience in predictive modeling using RWD to identify at risk patient populations with a publication record in peer-review journals
  • Experience in patient & healthcare provider segmentation to inform Medical and Commercial strategy
  • Demonstrated expertise in epidemiological study design and statistical methods such as propensity score matching, descriptive statistics, regression analysis, predictive modelling
  • Strong proficiency in statistical programming languages: SQL, Python, R, and/or SAS
  • Solid working knowledge of Snowflake for database querying and data extraction
  • Familiarity with medical coding systems: ICD-10, CPT, SNOMED CT, LOINC, RxNorm and experience/knowledge on OHDSI OMOP CDM standardized data model for healthcare data
  • Understanding of US EHR, claims, disease registry data, public health surveillance data as well as US healthcare billing system
  • Experience with AI coding tools such as Cursor, GitHub Copilot, Claude, LLM
  • Knowledge of automation tools such as Power Automate, Power App (an asset not required)
  • Requires a high level of interactive communication with diverse stakeholders
  • Can work with assumptions & in a fast-paced environment
  • Proven teamwork and collaboration skills

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