Consultant – Pharmacoepidemiologist

Ividata Life Sciences

. Coordinate the delivery of RWE and pharmacoepidemiological studies, from study design through delivery, either internally or in collaboration with CROs and external partners .

Posted 10/22/2026full-timeParis • FranceMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating real-world evidence (RWE) and pharmacoepidemiological studies, with a strong focus on study design, regulatory compliance, and scientific documentation. Proficient in managing CROs and overseeing project execution while ensuring adherence to quality standards and timelines.

Highest-signal resume keywords

Epidemiology ExpertisePharmacoepidemiological MethodologiesCRO ManagementScientific WritingHealthcare Database Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Study Design SelectionBias AssessmentStatistical Analysis PlansHealthcare Data-Source MappingFeasibility AnalysesRegulatory ProceduresBudget ManagementProject Timeline ManagementReal-World Data (RWD) Study DesignsQuality Framework Knowledge

Soft Skills

Analytical ThinkingDetail-OrientedOral CommunicationWritten CommunicationCross-Functional Collaboration

Tools & Technologies

SNDSEHR DatabasesHealthcare Registries

Certifications & Qualifications

Master's DegreePh.D.Doctor of PharmacyDoctor of Medicine

Industry Keywords

Real-World Evidence (RWE)PharmacoepidemiologyPublic HealthClinical ResearchPharmaceutical Industry

About the role

Key responsibilities & impact

Coordinate the delivery of RWE and pharmacoepidemiological studies, from study design through delivery, either internally or in collaboration with CROs and external partners
Serve as the operational and scientific point of contact for project teams and key stakeholders
Provide methodological expertise in epidemiology, including study design selection, healthcare database selection, bias assessment, and interpretation of results
Draft and review scientific documentation, including protocols, statistical analysis plans, study reports, abstracts, manuscripts, and presentations
Oversee the operational execution of projects, including CRO oversight, quality, regulatory procedures, budgets, and timelines
Conduct feasibility analyses, literature reviews, and healthcare data-source mapping
Contribute to the continuous improvement of RWD/RWE standards, methodologies, and best practices

Requirements

What you’ll need

Education: Master's degree, Ph.D., or Doctor of Pharmacy / Medicine degree with a specialization in Epidemiology, Pharmacoepidemiology, or Public Health
At least 3–5 years of clinical/academic or pharmaceutical industry/CRO experience in a similar RWE or epidemiology role
Strong command of pharmacoepidemiological methodologies and real-world data (RWD) study designs
Experience managing and overseeing CROs, monitoring budgets, and managing project timelines
Strong scientific writing skills, including protocols and publications
Knowledge of healthcare databases, particularly SNDS, registries, and EHR databases
Knowledge of the regulatory and quality framework governing RWE studies
Ability to work across a range of therapeutic areas
Rigorous and detail-oriented, with excellent oral and written communication skills, scientific leadership, analytical thinking, and the ability to work effectively cross-functionally
Fluency in written and spoken English is required

Benefits

Comp & perks

Hybrid working arrangement with remote work options
Stimulating and collaborative environment
High-impact assignments at the forefront of innovation in the Life Sciences
Collaboration with passionate experts
Opportunities to work with pharmaceutical companies, biotech firms, medical device companies, animal health, cosmetics, and nutrition organizations