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Real World Evidence Project Manager Jobs (NOW HIRING)

$160K - $200K/yr

You will be the senior epidemiological voice at Novellia, shaping how we design and deliver real-world evidence studies, building the methodological infrastructure the team will run on, and joining ...

## Sales Consultant Real World Evidence (m/w/d)Applylocations: Waldemstime type: Full timeposted on: Posted 3 Days Agojob requisition id: JR109805**Deine Aufgabe bei CGM:** Als führendes Unternehmen im ...

As a management consulting and technology firm focused on improving life and how we live it, we ... Work closely with project leadership, HEOR scientists, and cross-functional teams to understand ...

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Real World Evidence Project Manager information

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$44.5K

$96.6K

$154.5K

How much do real world evidence project manager jobs pay per year?

As of Sep 14, 2026, the average yearly pay for real world evidence project manager in the United States is $96,560.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,000.00 and $113,000.00 per year, depending on experience, location, and employer.

What is a real world evidence project manager?

A Real World Evidence (RWE) Project Manager oversees the planning, execution, and delivery of projects that use real-world data to generate evidence about the usage and outcomes of healthcare products. They coordinate multidisciplinary teams, manage timelines and budgets, and ensure compliance with regulatory and quality standards. The RWE Project Manager works closely with stakeholders to design studies, collect and analyze data, and communicate findings to inform clinical, regulatory, or market access decisions.

What are the key skills and qualifications needed to thrive as a real world evidence project manager?

To thrive as a Real World Evidence (RWE) Project Manager, you need a background in life sciences or public health, strong project management experience, and expertise in real-world data methodologies. Familiarity with data analytics platforms (such as SAS, R, or Python), regulatory requirements, and project management tools like MS Project or Jira is typically required. Excellent communication, leadership, and stakeholder management skills help you coordinate cross-functional teams and present complex findings clearly. These skills ensure efficient project delivery, regulatory compliance, and the generation of valuable insights that drive better healthcare decisions.

What are some common challenges faced by real world evidence project managers when working with cross-functional teams?

Real World Evidence (RWE) Project Managers often coordinate between diverse teams such as data scientists, clinicians, regulatory affairs, and external partners. One key challenge is aligning varying priorities and timelines while ensuring data quality and compliance with regulatory standards. Effective communication and proactive stakeholder management are essential to address data privacy issues, interpret complex real-world data, and keep projects on track. Building strong relationships and setting clear expectations early in the project can help navigate these challenges successfully.

What is the difference between Real World Evidence Project Manager vs Clinical Data Manager?

AspectReal World Evidence Project ManagerClinical Data Manager
Primary FocusManaging real-world evidence studies, data collection, and analysis for healthcare insightsDesigning, validating, and managing clinical trial data for regulatory submissions
Required CredentialsOften requires a background in healthcare, epidemiology, or related fields; certifications like RAC may be beneficialTypically requires a degree in life sciences, with certifications like CDM or CDISC standards
Work EnvironmentPharmaceutical companies, healthcare organizations, or research firmsClinical research organizations, pharmaceutical companies, or CROs

The Real World Evidence Project Manager focuses on managing studies that utilize real-world data to generate healthcare insights, while the Clinical Data Manager concentrates on handling clinical trial data for regulatory purposes. Both roles require strong data management skills but differ in their data sources and study types.

What cities are hiring for Real World Evidence Project Manager jobs?

Cities with the most Real World Evidence Project Manager job openings:

What states have the most Real World Evidence Project Manager jobs?

States with the most job openings for Real World Evidence Project Manager jobs include:

What are popular job titles related to Real World Evidence Project Manager jobs?

For Real World Evidence Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Real World Evidence Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $96,560 per year, or $46.4 per hour.

Senior Epidemiologist, Real-World Evidence

On-site

$160K - $200K/yr

Other

Medical, Dental, Vision, Retirement

Posted 21 days ago


Job description

ABOUT NOVELLIA

Novellia is the first and only company that lets anyone in the U.S. gain access to nearly a decade of their health data in under 30 seconds — 100% free. All your health records, across every doctor, in one place, always up to date.

We are the only patient-powered real-world data platform delivering comprehensive, patient-authorized longitudinal health insights to accelerate biopharma innovation. Unlike traditional RWD providers who deliver fragmented institutional data, we empower patients to access 20+ years of their health records, then transform these complete health journeys into fit-for-purpose datasets for evidence generation, regulatory submissions, and market access. We are growing 5x year over year, have raised close to $30M in funding, and are backed by tier-1 investors including Spark Capital, Khosla Ventures, and Bling Capital.

Working with the world's top researchers, we turn health insights into life-changing action for millions of people around the world.

THE ROLE

This is a founding scientific hire. You will be the senior epidemiological voice at Novellia, shaping how we design and deliver real-world evidence studies, building the methodological infrastructure the team will run on, and joining client and business development conversations as a scientific credibility anchor.

In the near term, this role is hands-on: you will design and execute studies in close collaboration with our data and biostatistics team while also helping us win new business by demonstrating scientific depth in early client conversations. As the team scales, you will move into a leadership role, setting quality standards and overseeing a growing group of epidemiologists.

We are looking for someone who has spent time at a pharma services firm, CRO, or health tech company and knows what good looks like in study design, client relationships, and scientific rigor. The ideal candidate is also technical, has strong command in AI coding and can independently design and execute on studies in collaboration with the broader team.

WHAT YOU'LL DO
  • Lead the design and execution of real-world evidence studies across natural history, comparative effectiveness, HEOR, treatment patterns, and external control arms
  • Partner with the commercial team on client and business development calls and execution of client-facing data and analytics services deliverables
  • Leverage AI tools to drive efficiency across the research workflow, from protocol structuring and literature synthesis to output generation, so you and the team can run multiple studies in parallel without sacrificing rigor.
  • Design and operationalize the plan to scale the research team, including headcount growth, SOP, analytics and client engagement playbook, in order to support leading biopharma clients with their evidence generation needs.
  • Collaborate closely with our data team on end-to-end delivery and mentor future scientific hires
  • Contribute to publications, conference presentations, and other scientific communications that build Novellia's external credibility
WHAT WE'RE LOOKING FOR
  • Master or PhD in epidemiology, pharmacoepidemiology, or a closely related field
  • 7+ years of RWE research experience in a pharma services, CRO, or health tech setting, not primarily academic
  • Deep familiarity with real-world data sources (EHR, claims, registries) and core study designs (cohort, case-control, external control arms, interrupted time series)
  • Comfortable engaging directly with pharma clients across medical affairs, HEOR, and clinical development, and able to lead scientific conversations with confidence
  • Strong command of causal inference methods, including propensity score methods, IPTW, and G-computation
  • An AI-forward mindset: you actively use AI tools to work faster and scale yourself, and are excited about what this means for scientific productivity
  • Published track record at conferences and in peer-reviewed journals
NICE TO HAVE
  • Experience in oncology, CVRM, or rare disease RWE
  • Exposure to regulatory-grade RWE for FDA or HTA submissions
  • Prior experience in an early-stage or startup environment
WHY NOVELLIA
  • You will be a foundational hire with the opportunity to build a scientific practice from the ground up. The infrastructure you create will define how this team operates for years.
  • You will work across a broad portfolio of pharma clients and therapeutic areas, with direct exposure to the full commercial cycle from BD to delivery
  • Competitive base salary ($160K–$200K), meaningful equity, and benefits
  • A team that takes scientific rigor seriously and invests in the tools and infrastructure to do the work well
Benefits & Perks
  • Equity in Novellia
  • Medical, dental, and vision coverage
  • 401(k)
  • Flexible time off
  • Wellness stipend
  • Up to 12 weeks of parental leave
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