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Real World Evidence Rwe Jobs in Boston, MA (NOW HIRING)

Vrtx

AI & Real World Analytics Senior Manager

Boston, MA · Hybrid

$148K - $223K/yr

Lead the design, execution, and delivery of Real-World Evidence (RWE) analysis projects, incorporating AI/ML methodologies * Optimize and complete processes such as analytics project workflows and ...

Merck Group

Director, HEOR - Rare Tumor

Boston, MA · On-site

$185K - $278K/yr

Developing comprehensive value evidence strategies - design and execute systematic literature reviews, real-world evidence (RWE) studies, and patient-reported outcomes (PRO) research to build a ...

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Real World Evidence Rwe information

What is the difference between Real World Evidence Rwe vs Clinical Data Analyst?

AspectReal World Evidence RweClinical Data Analyst
Required credentialsTypically requires a background in healthcare, epidemiology, or biostatistics, often with a master's or PhDUsually requires a degree in health informatics, biostatistics, or related fields, with similar certifications
Work environmentPrimarily in healthcare, pharmaceutical, or research organizations analyzing real-world dataIn clinical research settings, hospitals, or pharmaceutical companies analyzing clinical trial data
Employer and industry usageUsed by pharma companies, healthcare providers, and research institutions to generate real-world insightsUsed by research organizations, hospitals, and pharma for clinical trial data management and analysis

Real World Evidence Rwe professionals focus on analyzing data from real-world settings like electronic health records and insurance claims, while Clinical Data Analysts primarily work with clinical trial data. Both roles require strong analytical skills and related credentials, but Rwe specialists emphasize real-world data sources to inform healthcare decisions.

What is real world evidence (RWE)?

Real World Evidence (RWE) refers to clinical evidence regarding the usage and potential benefits or risks of a medical product, derived from analysis of real-world data (RWD). This data is collected from sources outside of traditional clinical trials, such as electronic health records, insurance claims, patient registries, and wearable devices. RWE plays a crucial role in understanding how treatments work in routine clinical practice, informing regulatory decisions, and supporting drug development and market access. Organizations use RWE to complement clinical trial data, improving healthcare outcomes and patient care.

What are the key skills and qualifications needed to thrive as a real world evidence (RWE) professional?

To thrive as a Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, and data analysis, often supported by an advanced degree in a relevant scientific field. Familiarity with statistical software (such as SAS, R, or Python), real-world data sources (like EHRs and claims databases), and regulatory guidelines (FDA/EMA) is essential. Strong communication, problem-solving, and cross-functional collaboration skills help convey complex findings to stakeholders and integrate RWE into decision-making. These competencies are crucial for generating credible insights that inform clinical, regulatory, and commercial strategies in the healthcare industry.

How does a real world evidence (RWE) professional collaborate with cross-functional teams?

RWE professionals often work closely with colleagues from epidemiology, health economics, medical affairs, and regulatory affairs to design and execute studies using real-world data. Collaboration is essential, as RWE findings support evidence generation for regulatory submissions, market access, and post-marketing surveillance. Regular meetings, data-sharing sessions, and joint project planning are common, ensuring all stakeholders are aligned on study objectives, methodologies, and data interpretation. This collaborative environment helps translate complex data into actionable insights that support decision-making across the organization.

What are the most commonly searched types of Real World Evidence Rwe jobs in Boston, MA?

The most popular types of Real World Evidence Rwe jobs in Boston, MA are:

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For Real World Evidence Rwe jobs in Boston, MA, the most frequently searched job titles are:

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Real World Evidence Rwe jobs near you
Infographic showing various Real World Evidence Rwe job openings in Boston, MA as of August 2026, with employment types broken down into 83% Full Time, 9% Part Time, 2% Temporary, and 6% Contract. Highlights an 77% In-person, 8% Hybrid, and 15% Remote job distribution.

Solutions and Market Lead (Pharma - Medical Affairs, Market Access, HEOR, & RWE)

trinetx1

Cambridge, MA • On-site, Remote

Full-time

Re-posted 3 days ago

Job description

POSITION TITLE:  Solutions and Market Lead (Pharma – Medical Affairs, Market Access, HEOR, & RWE) 

LOCATION: Cambridge, MA (hybrid) or U.S. (remote) 

This position reports to our global HQ in Cambridge, MA. Travel is expected domestically and internationally when needed.

 

Who We Are: 

TriNetX connects healthcare organizations and researchers across the globe so they can see what’s happening in real patient populations—not guesses, not simulations.

Our aim is simple and ambitious: Provide a clear path to trustworthy answers, whether your goal is to create promising new therapies, publish groundbreaking research, or improve health outcomes.

We keep identifiable data where it belongs—inside more than 11,000+ clinical sites across 20+ countries—preserving security, provenance, and granularity. Our trusted partnerships with providers ensure high-fidelity data, and a properly governed linkage back to individual patients.

At TriNetX, we enable life sciences, healthcare, and academic institutions to strengthen human health—with data you can trace, evidence you can defend, and answers you can trust.

Who We Are Looking For: 

The Solution and Market Lead for Medical Affairs, Market Access, HEOR, and Real World Evidence (RWE) is accountable for owning the solution strategy, market positioning, and commercial success of offerings that support evidence generation, value demonstration, and patient access across the pharmaceutical lifecycle. 

This role serves as the market owner and domain authority for post-approval and peri-approval evidence use cases, translating the needs of Medical Affairs, HEOR, Market Access, and Value & Outcomes teams into scalable, differentiated solutions. The individual will work cross functionally with Product, Data, Delivery, Marketing, and Commercial teams to ensure solutions are scientifically credible, commercially compelling, and aligned with evolving payer, HTA, and regulatory expectations. 

They will be responsible for understanding and communicating market problems/hassles and working with our Product Management, Client Delivery, and Commercial teams to devise, build, sell, and deliver existing and new solutions.

This role will report into our SVP, Solutions and Product Management and join a team of fellow market owners.  
 

What You Will Be Doing:

  • Market & Customer Leadership 
    • Own deep expertise in Medical Affairs, HEOR, Market Access, and RWE workflows, including value story development, comparative effectiveness, burden of illness, outcomes research, and payer/HTA evidence requirements.  
    • Maintain a current view of payer, HTA, and regulatory evidence expectations across key geographies and therapeutic areas.  
    • Define buyer personas (e.g., Medical Affairs, HEOR, Value & Access, Epidemiology, Evidence Generation) and articulate their success metrics and pain points.
  • Solution Strategy & Lifecycle Ownership 
    • Lead endtoend solution ownership from ideation and design through prelaunch, launch, and postlaunch optimization, in alignment with the broader solution/product management framework. 
    • Partner closely with Product, Data, Engineering, and Delivery teams to shape solution scope, differentiation, and scalability. 
    • Define solution packaging, pricing inputs, and value articulation for the associated pharma use cases. 
  • Go-to-Market & Commercial Enablement 
    • Develop and execute the GTM strategy for Medical Affairs, Market Access, HEOR, and RWE solutions within pharma. 
    • Enable Sales, Account Management, and Customer Success with messaging, pitch materials, usecase narratives, and competitive positioning. 
    • Support complex deals by participating in discovery, shaping solution approaches, and engaging credibly with senior medical and access stakeholders.
  • Revenue & Impact Accountability 
    • Own pipeline influence, bookings contribution, and adoption metrics for the solution portfolio.  
    • Balance near term commercial opportunities with longer term platform and capability investments.  
    • Track post sale usage and outcomes to refine solution-market fit and expand footprint within accounts. 
  • Cross Functional & Thought Leadership 
    • Serve as the connective tissue between market needs and internal execution across Product, Delivery, Commercial, and Marketing teams. 
    • Ensure scientific rigor, methodological credibility, and compliance considerations are embedded in solution design and positioning. 
    • Act as an internal and external thought leader on the role of RWE, HEOR, and value evidence in modern pharma decision making. 

What You Bring to TriNetX:

  • 10+ years of experience in Medical Affairs, HEOR, Market Access, RWE, or outcomes research within pharma, biotech, CROs, or evidence/data vendors.  
  • Demonstrated experience owning solution strategy, market ownership, or product adjacent leadership in a life sciences B2B environment.  
  • Strong understanding of real world data sources, study designs (retrospective and prospective), and evidence generation for regulatory, payer, and HTA use.  
  • Proven ability to work cross functionally and influence senior stakeholders without direct authority.  

Bonus Points:

  • Advanced degree (PhD, PharmD, MPH, MSc, MD) or equivalent experience in epidemiology, health economics, outcomes research, or related fields.
  • Experience launching or scaling new RWE, HEOR, or value focused solutions.  
  • Comfort engaging with senior Medical Affairs, HEOR, and Market Access leaders at global pharma companies. 
 
 

Learn More About TriNetX:

To learn more about us, please check out our website, blog, and Careers page - and be sure to follow us on  LinkedIn. 

 

Interested In Joining Our Community?

TriNetX is an Equal Opportunity Employer. All persons are considered for employment without regard to their race, color, creed, religion, national origin, ancestry, citizenship status, age, disability or handicap, sex or gender, marital status, sexual orientation, genetic information, gender identity, veteran status, or any other characteristic or status protected by applicable federal, state or local laws.

 

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