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Consultant – Real-World Evidence Strategy Lead
Ividata Life Sciences. Define and lead the RWE scientific strategy in alignment with the integrated evidence generation plan, Medical Affairs, Market Access, and R&D .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Expertise in Real-World Evidence (RWE) scientific strategy, including study design, statistical analysis, and observational methods, with a strong focus on collaboration across pharmaceutical and biotechnology sectors. Proficient in translating scientific results into strategic messages for regulatory and health authorities.
Highest-signal resume keywords
PhD In Public HealthObservational Study Protocol DevelopmentAdvanced Proficiency In Healthcare DatabasesEpidemiological Bias ManagementComplex Observational Analysis Methods
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
RWE Scientific StrategyStatistical Analysis PlansPICOT FrameworkStudy Design SelectionData Source SelectionPredictive ModelingMethodological Quality AssuranceScientific CommunicationObservational MethodsIndirect Comparisons
Soft Skills
Critical ThinkingNegotiation SkillsInterpersonal Abilities
Industry Keywords
Pharmaceutical SectorBiotechnology SectorHealth AuthoritiesMedical AffairsMarket AccessR&D
About the role
Key responsibilities & impact- Define and lead the RWE scientific strategy in alignment with the integrated evidence generation plan, Medical Affairs, Market Access, and R&D
- Structure the scientific approach for RWE studies, including the PICOT framework, study design selection, and data source selection
- Oversee the development of statistical analysis plans in collaboration with biostatisticians
- Ensure the methodological quality of protocols, reports, publications, and scientific communications
- Provide expertise in observational methods, bias, adjustment techniques, indirect comparisons, and predictive modeling
- Translate scientific results into strategic messages for regulatory bodies, health authorities, payers, and the medical community
- Scientifically evaluate and validate RWE initiatives conducted by affiliates within cross-functional teams
- Collaborate with clients in the pharmaceutical and biotechnology sectors
Requirements
What you’ll need- PhD in Public Health, Epidemiology, Pharmacoepidemiology, or Health Economics—or an MD/PharmD degree
- Demonstrated experience as the lead author of at least one observational study protocol, with overall responsibility for its methodological design and study design
- Advanced proficiency in healthcare databases
- Advanced proficiency in complex observational analysis methods
- Strong command of epidemiological bias management
- Critical thinking skills and the ability to challenge and refine scientific objectives
- Excellent negotiation skills and strong interpersonal abilities when engaging with diverse stakeholders
- Fluency in written and spoken English is essential
Benefits
Comp & perks- Stimulating and collaborative environment
- High-impact assignments focused on healthcare innovation
- Possibility of hybrid working
- Collaboration with experts and leading organizations in the pharmaceutical, biotechnology, medical device, animal health, cosmetics, and nutrition sectors