Clinical Data Scientist

Reference no. R2853801

Job Title:  Clinical Real World Data Scientist

Department: Digital RWD & Health Intelligence (Digital RWD & HI)

Location: Toronto, ON

About the Job

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 has the right data, used the right way, for real patient impact.

The CoE is responsible for:

Establishing and maintaining enterprise-wide standards for RWD assessment and fitness-for-purpose data evaluation through the Data Insights & Viability Engine (DIVE).

Supporting cross-functional teams, including R&D, Business units (Vaccines, General Medicine and Specialty Care) & Digital, with expert guidance on data source selection & suitable data usage to minimize bias and confounder.

Building and disseminating best practices, methodological frameworks, and training resources across Sanofi's RWD ecosystem

Driving innovation in RWD methodologies, including the integration of AI tools such as Cursor, LLM, CortexAI (as available) to accelerate speed to delivery of data selection guidance, internal study design, and/or digital product development

The Clinical RWD Scientist is a critical role within the Data Assessment Center of Excellence (CoE), embedded in Sanofi's Digital RWD & HI function. This role bridges the gap between theoretical concepts to practical & reliable RWD solutions.  You are an agile professional interested in challenging the status quo with deep subject matter expertise in US RWD, pharmaco-epidemiological methods and a quick learner of new data, methodology, and technology. You are a proactive team member that values cross-learning, see challenges as opportunity and can work with assumptions.

About Sanofi

We’re   an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main Responsibilities

You will be responsible for designing and executing rigorous data assessment frameworks, evaluating the fitness-for-purpose of real-world data (RWD) sources for insights or evidence generation across the enterprise, support the development of reliable RWD Foundation and Products. The Applied RWD Scientist serves as a methodological authority and RWD data domain expert, ensuring best-in-class data selection and optimal data usage to generating reliable insights or evidence.  This role is key to ensure data-drive decision is reliable, trustworthy, and timely.

Data Assessment & Fitness-for-Purpose Evaluation

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

Methodological Design & Optimal RWD Usage

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

Cross-Functional Collaboration & Stakeholder Engagement

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

NOTE: This role does not conduct real-world evidence studies.

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

Why Choose Us?  

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether   it’s   through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take   good care   of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare,   prevention   and wellness programs and at least   14 weeks ’ gender-neutral parental leave

Applications received after the official close date will be reviewed on an individual basis.​

This position is for a new vacant role that is now open for applications.​ 

AI Usage

"Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company’s Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal,   Data Subject Rights Webform . The  Data Subject Rights Webform  can also be used to request access or correction of your personal information and file a complaint.

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants.  Accommodations for persons with disabilities required during the recruitment process are available upon request.

#GD-SP ​

#LI-SP

#LI-Onsite

#DBBCA

Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

North America Applicants Only

The salary range for this position is:

127,000.00 - 177,000.00 (Includes target bonus) Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefits programs, and additional benefits information can be found through the (CA) LINK OR (US) LINK .

La fourchette salariale pour ce poste est la suivante:

127,000.00 - 177,000.00 (Comprend le bonus cible) La rémunération finale sera déterminée en fonction de l'expérience démontrée, des compétences, du lieu de travail et d'autres facteurs pertinents. Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise, et des informations supplémentaires sur les avantages sociaux peuvent être trouvées via le lien