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Excelya

RWE Scientist

Excelya

. Lead the operational and scientific execution of assigned Real-World Evidence (RWE) studies and projects .

Posted 10/23/2026full-timeSaclay • FranceMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Real-World Evidence and pharmacoepidemiology, with a strong focus on designing and executing observational studies. Proficient in project management and collaboration with external partners while ensuring adherence to regulatory requirements and methodological standards.

Highest-signal resume keywords
Real-World Evidence ExpertisePharmacoepidemiologyProject ManagementEpidemiological MethodologiesFluent Professional English

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Pharmacoepidemiological Study DesignData AnalysisFeasibility StudiesLiterature ReviewsStatistical Analysis PlansHealth Database AnalysisStudy Protocol DevelopmentResults InterpretationQuality OversightBudget Management
Soft Skills
CommunicationCollaborationLeadership
Certifications & Qualifications
Master’s DegreePharmDMDPhD
Industry Keywords
Real-World DataObservational StudiesHealth DatabasesRegulatory RequirementsScientific Documentation

About the role

Key responsibilities & impact
  • Lead the operational and scientific execution of assigned Real-World Evidence (RWE) studies and projects
  • Serve as the primary point of contact for internal teams and external stakeholders on RWE projects
  • Design and implement pharmacoepidemiological studies using real-world data
  • Provide methodological expertise on study designs, data sources, potential biases, and interpretation of results
  • Conduct feasibility studies, literature reviews, and analyses of available health databases
  • Oversee CROs and external partners, including protocols, deliverables, quality, budgets, and timelines
  • Draft and review scientific documents, including protocols, statistical analysis plans, study reports, abstracts, publications, and presentations
  • Contribute to the continuous improvement of standards and best practices

Requirements

What you’ll need
  • Master’s degree, PharmD, MD, or PhD in Epidemiology, Pharmacoepidemiology, Public Health, Biostatistics, or an equivalent scientific discipline
  • Proven expertise in Real-World Evidence, pharmacoepidemiology, or applied epidemiology
  • Experience designing and leading observational studies
  • Expertise in RWE/RWD
  • Project management skills and experience overseeing external partners
  • Strong understanding of epidemiological methodologies, health databases, and related regulatory requirements
  • Fluent professional English required
  • Fluent professional French required

Benefits

Comp & perks
  • Inclusive, diverse, and equitable work environment
  • Equal opportunity
  • Professional development
  • Diverse, high-impact projects
  • Collaboration with recognized experts
  • Integrated service model (Resourcing, Functional Service Provider, and Full Service)
  • Contribution to improving the patient journey