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Internship Real World Evidence Rwe Jobs in Roxbury, MA

Vrtx

AI & Real World Analytics Senior Manager

Boston, MA · Hybrid

$148K - $223K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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

  • Medical

  • Retirement

  • PTO

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 ...

Ipsen Group

Director, Epidemiology & RWE Sciences

Cambridge, MA · On-site

$177 - $259.60/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Real-World Evidence Generation:*** Design prospective and retrospective pharmaco-epidemiology studies (including RWE studies) in the pre-/post-launch setting, including related to Regulatory post ...

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Internship Real World Evidence Rwe information

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How much do internship real world evidence rwe jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for internship real world evidence rwe in Roxbury, MA is $16.87, according to ZipRecruiter salary data. Most workers in this role earn between $13.56 and $19.04 per hour, depending on experience, location, and employer.

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

To thrive as an Internship Real World Evidence (RWE) professional, you need a solid background in life sciences, epidemiology, or statistics, often supported by progress toward a relevant degree. Familiarity with data analysis tools like SAS, R, or Python, and experience with healthcare databases or real-world data systems, are typically required. Strong analytical thinking, attention to detail, and collaborative communication skills help interns excel in cross-functional teams and data-driven projects. These competencies are crucial for generating robust, actionable insights from real-world data to inform healthcare decisions and policy.

What is an internship in real world evidence (RWE)?

An Internship in Real World Evidence (RWE) offers students or recent graduates hands-on experience in collecting and analyzing data from real-world sources, such as electronic health records, insurance claims, and patient registries. RWE is used in the pharmaceutical and healthcare industries to evaluate the effectiveness, safety, and value of medical treatments outside controlled clinical trials. Interns may support research studies, help interpret data, and contribute to reports that inform decision-making for healthcare providers and regulators. This type of internship is ideal for those interested in data analysis, public health, and evidence-based medicine.

What types of projects do interns typically work on in a real world evidence (RWE) internship?

As an RWE intern, you can expect to contribute to projects involving the collection, analysis, and interpretation of real-world healthcare data, such as electronic health records, claims data, or patient registries. Common responsibilities include supporting data cleaning, conducting literature reviews, assisting with statistical analyses, and preparing reports or presentations for internal teams. You will often collaborate with cross-functional teams including epidemiologists, data scientists, and medical affairs professionals, which provides excellent exposure to various aspects of the pharmaceutical or healthcare industry.

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

AspectInternship Real World Evidence RweData Analyst
Required CredentialsTypically pursuing or recent graduate in healthcare, life sciences, or related fieldsBachelor's degree in statistics, mathematics, computer science, or related fields
Work EnvironmentHealthcare or pharmaceutical companies, research organizations, or academic institutionsVarious industries including finance, healthcare, marketing, and technology
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare sectors for evidence generationWidely used across multiple industries for data analysis and reporting

While both roles involve working with data, an Internship Real World Evidence Rwe focuses on analyzing real-world healthcare data to generate evidence for medical decisions, often within healthcare or pharma settings. A Data Analyst has a broader scope, working with various data types across industries to interpret and visualize data for business insights.

What cities near Roxbury, MA are hiring for Internship Real World Evidence Rwe jobs?

Cities near Roxbury, MA with the most Internship Real World Evidence Rwe job openings:

Internship Real World Evidence Rwe jobs near you
Infographic showing various Internship Real World Evidence Rwe job openings in Roxbury, MA as of August 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution, with an average salary of $35,089 per year, or $16.9 per hour.

Medical Director, US Medical Affairs

Dyne Therapeutics

Waltham, MA • On-site

Full-time

Re-posted 21 days ago

Job description

Role Summary:

The US Medical Director of Medical Affairs leads Dyne's medical strategy and execution within the United States, focusing on launch readiness, US-specific KOL engagement, congress planning and execution, and supports real-world evidence (RWE) initiatives. This role ensures alignment with global strategy while tailoring activities to US regulatory, payer, and healthcare landscapes. This role leads efforts to communicate and disseminate scientific and clinical information, engage with medical professionals in the field and contribute to the overall success of the company's portfolio. The US Medical Director collaborates closely with Global Medical Affairs, US Commercial, Regulatory, Market Access, and Clinical teams to drive successful product introduction and lifecycle management in the US market.  

This role is located in our Waltham, MA office.

Primary Responsibilities Include: 

  • Develop and execute US Medical Affairs strategy aligned with global objectives and US market needs 
  • Act as point person for all US Medical Affairs launch readiness activities, including working closely with global medical director and scientific communications on development of scientific platform development, local congress planning, and local medical education programs 
  • Support congress strategy execution in the US, including booth activities, symposia, and scientific presentations 
  • Work closely and with the Head of the Medical Science Liaison (MSL) team on US KOL engagement strategy: identify, map, and build relationships with key US experts 
  • Support insight collection and synthesis, and supporting the development of field material, working with the MSL team 
  • Develop US Medical Affairs advisory board strategy and organize and execute advisory boards and expert panels 
  • Work collaboratively with HCP and Patient Marketing as well as cross-functional stakeholders to integrate medical perspectives into brand strategy, ensuring alignment with scientific and commercial objectives 
  • Partner with Clinical Development and Clinical Operations to support US trial site engagement and recruitment strategies 
  • Working with the Global Medical Director, identify opportunities to generate real-world evidence (RWE) and phase IV data to address data gaps and support HCP and payer treatment decisions 
  • Ensure compliance with US regulatory and legal requirements for all medical activities 
  • Serve as subject matter expert on neuromuscular diseases and Dyne's therapeutic platforms for US stakeholders 
  • Support the review and approval of externally presented materials through the Medical Review committee and Promotional Review Committee  
  • Act as a role model for integrity and compliance in all interactions 

Education and Skills Requirements: 

  • Doctorate degree (MD, PhD, PharmD) with experience in rare diseases; neuromuscular experience preferred 
  • Minimum 8 years of relevant experience in Medical Affairs within the US pharmaceutical/biotech industry 
  • Proven ability to lead US launch readiness and medical strategy execution 
  • Excellent communication and relationship-building skills with US KOLs and cross-functional teams 
  • Ability to interpret and communicate complex scientific data to diverse audiences 
  • Effective communication skills (written, verbal and presentation) 
  • Must be willing to travel up to 30%, inclusive of overnight and occasional weekends to meet with customers, internal stakeholders and attend relevant conferences  
  • Candidates must be authorized to work in the U.S. 
  • Positive team member who embodies Dyne's Core Values 
  • Excitement about Dyne's vision and mission  
  • Experience managing direct reports  

Apply