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Vice President Real World Evidence Rwe Jobs (NOW HIRING)

UCB

RWE Strategy Lead, Developed Brands

Boston, MA

About the Role You will lead the development and execution of global real-world evidence (RWE) strategies that support the value, safety, effectiveness, and patient impact of UCB's therapies. You ...

New

UCB

RWE Strategy Lead, Developed Brands

Boston, MA · On-site

About the Role You will lead the development and execution of global real-world evidence (RWE) strategies that support the value, safety, effectiveness, and patient impact of UCB's therapies. You ...

ZS

Medical & Evidence Manager

Boston, MA · On-site

... Clinical Operations, Real-World Evidence (RWE), Medical Affairs, Payers, Providers, and ... to VP and C-suite client stakeholders, helping shape strategic decisions through data-driven ...

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Vice President Real World Evidence Rwe information

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$157.5K

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How much do vice president real world evidence rwe jobs pay per year?

As of Aug 6, 2026, the average yearly pay for vice president real world evidence rwe in the United States is $157,532.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,000.00 and $190,000.00 per year, depending on experience, location, and employer.

What is the difference between Vice President Real World Evidence Rwe vs Director Real World Evidence Rwe?

AspectVice President Real World Evidence RweDirector Real World Evidence Rwe
CredentialsAdvanced degrees (PhD, MD, or equivalent), extensive experience in RWEMaster's or PhD, relevant industry experience
Work EnvironmentStrategic leadership, cross-functional oversightOperational management, project execution
Industry UsageExecutive-level RWE strategy roles in pharma/biotechMid-level RWE project management roles

The Vice President Real World Evidence Rwe typically holds a senior leadership role, focusing on strategic RWE initiatives and overseeing teams, while the Director Real World Evidence Rwe manages day-to-day RWE projects and teams. Both roles require relevant credentials and industry experience, but differ mainly in scope and responsibility.

What cities are hiring for Vice President Real World Evidence Rwe jobs? Cities with the most Vice President Real World Evidence Rwe job openings:
What are the most commonly searched types of Real World Evidence Rwe jobs? The most popular types of Real World Evidence Rwe jobs are:
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Vice President Real World Evidence Rwe jobs near you
Infographic showing various Vice President Real World Evidence Rwe job openings in the United States as of August 2026, with employment types broken down into 78% Full Time, 19% Part Time, and 3% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $157,532 per year, or $75.7 per hour.

Associate Director, Real World Evidence (RWE) Science

Ubertal Inc

Waltham, MA • Remote

Contractor

Re-posted 21 days ago

Job description

Job Title: Associate Director, Real World Evidence (RWE) Science – Phase IV / Post-Approval (Contract)

Location: United States (Remote; Eastern Time business hours preferred)
Duration: 7-Month Contract (Full-Time, 40 hours/week)
Start: Targeting Early March 2026

We are seeking an experienced Associate Director, Real World Evidence (RWE) Science to provide coverage for a Phase IV / post-approval RWE portfolio within a global Medical Affairs environment. This is a senior-level individual contributor role requiring deep epidemiology and real-world evidence expertise, strong methodological leadership, and the ability to independently manage ongoing studies with minimal ramp-up.

This position supports global stakeholders, including Europe, and requires flexibility for early morning meetings aligned to EU collaboration.

Key Responsibilities

  • Lead scientific oversight of Phase IV and post-approval real-world evidence (RWE) and observational studies

  • Provide methodological and technical leadership for study design, feasibility assessments, and evidence planning (EU focus)

  • Oversee vendors/CROs conducting outsourced analyses; review protocols, statistical analysis plans, and outputs to ensure scientific rigor

  • Conduct and/or supervise systematic literature reviews (SLRs) and meta-analyses

  • Contribute to development of RWE plans aligned with regulatory, HTA, and post-approval commitments

  • Support retrospective analyses leveraging real-world data sources (claims, EHR, registries)

  • Guide protocol development for observational studies and pragmatic trials

  • Perform evidence reviews to inform regulatory submissions, reimbursement strategy, and medical strategy

  • Collaborate with Regional Medical Affairs on scientific exchange and external RWE engagement

  • Support development of abstracts, posters, manuscripts, and internal scientific communications

Required Qualifications

  • Advanced degree (MD, PhD, or MS) in Epidemiology, Biostatistics, Public Health, or related field

  • 8–10+ years of progressive experience in epidemiology and real-world evidence

  • Minimum 5 years of Pharma or Biotech industry experience

  • Strong expertise in:

    • Phase IV / post-approval epidemiologic study design

    • Retrospective real-world data (RWD) analyses

    • Observational research methodologies

  • Experience overseeing vendors/CROs and critically evaluating statistical methodologies

  • Proficiency with statistical software (R, SAS, Stata) and strong understanding of claims/EHR data structures

  • Demonstrated ability to work autonomously in a global, matrixed environment

  • Flexibility to support EU collaboration across time zones

Preferred Qualifications

  • Experience supporting regulatory or HTA-facing RWE deliverables

  • Vaccines, infectious disease, or public health epidemiology background

  • Experience with systematic literature reviews and meta-analyses

  • R programming skills, including simulations, power calculations, or Shiny applications

  • Experience with data extraction, cleaning, and standardization for RWD

  • Prior authorship of scientific publications and presentations

  • Experience supporting EU feasibility assessments and RWE expectations

Role Highlights

  • Senior-level RWE leadership without people management responsibilities

  • High-visibility Phase IV and real-world effectiveness portfolio

  • Global collaboration with strong EU engagement

  • Remote flexibility within the United States

Qualified candidates with deep RWE and epidemiology expertise, strong methodological grounding, and Phase IV experience in Pharma/Biotech are encouraged to apply.