Senior Epidemiologist, Inflammation, RWE & Regulatory Strategy

IQVIA

Conduct epidemiological research for Inflammation therapies at IQVIA, focusing on real-world evidence studies. Collaborate with stakeholders to enhance clinical development strategies based on findings.

Posted 6/29/2026full-timeRemote • Massachusetts, New York, North Carolina, Pennsylvania • 🇺🇸 United StatesSenior💰 $109,200 - $273,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in designing and executing Real World Evidence studies, with a strong focus on regulatory requirements and observational research methodologies. Proficient in collaborating with cross-functional teams to generate actionable insights from large healthcare datasets.

Highest-signal resume keywords

Doctoral Degree In EpidemiologyReal World Evidence Study DesignRegulatory Requirements UnderstandingObservational Research ExperienceCollaboration Across Cross-Functional Teams

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Real World Evidence StudiesStudy DesignData InterpretationHealthcare Dataset AnalysisEpidemiologic Expertise

Soft Skills

CollaborationIndependent Operation

Tools & Technologies

HealthVerityPharMetrics PlusTriNetX

Industry Keywords

InflammationLupusIBDCrohn’sClinical Development StrategySafety ProfilesPhase 2 ProgramsPhase 3 Programs

About the role

Key responsibilities & impact

Support a Real World Evidence team focused on Inflammation, with flexibility across indications (e.g., lupus, IBD, Crohn’s).
Design and execute real-world evidence (RWE) studies that inform clinical development strategy.
Generate evidence to address regulatory questions related to safety profiles and evidence gaps for Phase 2 and Phase 3 programs.
Provide scientific oversight across complex observational research, leveraging secondary data sources such as commercial real-world data platforms.
Apply epidemiologic expertise to study design, execution, and interpretation, focusing on fit-for-purpose evidence for regulatory and clinical decision-making.
Collaborate with cross-functional stakeholders, operating independently within a sponsor-dedicated environment.

Requirements

What you’ll need

Doctoral degree in Epidemiology
5–7 years of experience within a pharma company or pharma consulting environment
Experience conducting real-world evidence studies using secondary data sources, including commercial RWD platforms (e.g., HealthVerity, PharMetrics Plus, TriNetX)
Strong understanding of regulatory requirements supporting clinical development, including the types of evidence required to address safety and evidence gaps for Phase 2 and Phase 3 programs
Experience supporting clinical development and/or drug safety through observational research
Ability to work with and interpret large healthcare datasets; advanced programming not required
Strong ability to collaborate across cross-functional teams and contribute to study design, execution, and interpretation

Benefits

Comp & perks

Access IQVIA’s global network who supports your growth.
Be part of a forward-thinking team that helps shape the next generation of evidence-based healthcare.
Work hand-in-hand with one leading sponsor, gaining deep expertise in their therapies.
Opportunity to make an impact while building a career that matters.