1

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

This role will work directly within the Medical & Evidence Generation space, partnering closely with stakeholders across Drug Development, Clinical Operations, Real-World Evidence (RWE), Medical ...

The ideal candidate will have a strong background working with clinical trial data while also bringing experience supporting Real-World Evidence (RWE) initiatives and Medical Affairs projects. This ...

Director Epidemiology & RWE Sciences

Cambridge, MA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Title: Director Epidemiology & RWE Sciences Company: Ipsen Biopharmaceuticals Inc. About Ipsen ... The role is responsible for leading the global evidence strategy and real world evidence generation ...

Showing results 21-40

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:

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

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

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.

Director, US Health Economics and Outcomes Research & Real-World Evidence

Ipsen

Cambridge, MA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago


Job description

Title:

Director, US Health Economics and Outcomes Research & Real-World Evidence

Company:

Ipsen Biopharmaceuticals Inc.


About Ipsen:

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation.

Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company's success. Join us on our journey towards sustainable growth, creating real impact on patients and society!

For more information, visit us at https://www.ipsen.com/and follow our latest news on LinkedIn and Instagram.

Job Description:

WHAT - Summary & Purpose of the Position

The Director, US Health Economics and Outcomes Research (HEOR) & Real World Evidence (RWE) is responsible for identifying real-world and economic evidence needs and developing the real-world, clinical, humanistic, and economic evidence generation plans in collaboration with internal business partners to support the value of our products for US healthcare providers, population-health decision makers, and other external stakeholders for the assigned Therapeutic Area.

The Director, US HEOR & RWE will ensure scientific rigor in the design and conduct of US HEOR & RWE studies and the effective communication of results to internal and external audiences, including scientific exchange through publications. The Director of US HEOR & RWE will also partner cross-functionally to ensure that HEOR plans are strategically aligned across the organization including Brand Marketing, Medical Affairs, Value & Access, and Global RWE, and Global HEOR.

Additionally, the Director, US HEOR & RWE will support field team engagements by developing field team resources and by training field teams.

WHAT - Main Responsibilities & Technical Competencies

  • Drive effective cross-functional collaboration and lead the development of US HEOR evidence generation strategies in alignment with medical and commercial priorities, including strategies supporting products focused on the assigned conditions.
  • Provide input into Integrated Evidence Generation Plans to ensure US needs are represented.
  • Lead the design, conduct, and publication of methodologically rigorous US HEOR & RWE studies and projects, in collaboration with internal and external researchers.
  • Lead the development of materials, including AMCP dossiers, budget impact models, and value communication resources to support customer engagements.
  • Lead the training of customer-facing teams, such as US Medical Value Liaison (MVL), Value and Access, and MSL colleagues, on value communication resources to support customer engagements.
  • Support meetings with key external customers through participation in meetings or presenting approved value communication resources to customers as needed.
  • Provide input into clinical development programs and clinical trial protocols as needed.
  • Track budgets and timelines and ensure appropriate processes are followed for internal approval and execution of US HEOR projects.
  • Comply with all regulatory laws, regulations and policies that govern the conduct of Ipsen.
  • Stay informed on the latest methodological advances that expand and enhance HEOR research.

HOW - Knowledge & Experience

Knowledge & Experience (essential):

  • 8+ years of experience in Health Economics and Outcomes Research (HEOR), including presenting studies at scientific conferences and/or in a field role.
  • Demonstrated experience leading cross-functional teams or initiatives, and collaborating effectively with internal teams, external partners, and vendors.
  • Strong communication (oral and written), interpersonal, and project management skills, with the ability to influence without authority, build relationships with key stakeholders, and develop realistic plans and recommendations.
  • Proven ability to thrive in a fast-paced, dynamic environment by remaining flexible, proactive, and possess strong attention to detail.
  • Deep understanding of the US healthcare and payer landscape, including reimbursement systems, healthcare data assets, primary and secondary data collection, and health-system research capabilities.
  • Significant experience in the approval and delivery of proactive and reactive medical and scientific communications.
  • Track record of timely execution and completion of research and non-research deliverables.
  • Prior experience with product launches is desirable.
  • Ability to travel approximately 20-30% of the time.

Education / Certifications (essential):

  • Advanced degree (PhD, PharmD, MS, MPH) in Health Services Research, Health Economics, Epidemiology, Public Health, Pharmacy, or a related field is required.

Language(s) (essential):

  • Fluent in English.

Ipsen Biopharmaceuticals, Inc. is an equal opportunity employer. We recruit, employ, train, compensate, and promote without regard to race, religion, creed, national origin, age, gender, sexual orientation, sexual identity, marital status, military or veteran status, disability, genetic information, or any other category protected by applicable federal, state or local law.

Ipsen Biopharmaceuticals, Inc. conducts background screening, reference checks, and drug testing as part of its pre-employment screening process. This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned.

All Employees are expected to adhere to all company policies and act as a role model for company values.

The annual base salary range for this position is $190,000-$275,000.

This job is eligible to participate in our short-term incentives program as well as our long-term incentives program.

At Ipsen we are proud to offer a comprehensive employee benefits package, including 401(k) with company contributions, group medical, dental and vision coverage, life and disability insurance, short- and long-term disability insurance, as well as flexible spending accounts. Ipsen also provides parental leave, paid time off, a discretionary winter shutdown, well-being allowance, commuter benefits, and much more.

The pay range displayed above is the range of base pay compensation within which Ipsen expects to pay for this role at the time of this posting. Individual compensation within this range depends on a variety of factors, including, but not limited to, prior education and experience, job-related knowledge and demonstrated skills.

We are committed to creating a workplace where everyone feels heard, valued, and supported; where we embrace "The Real Us". The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities. When we include diverse ways of thinking, we make more thoughtful decisions and discover more innovative solutions. Together we strive to better understand the communities we serve. This means we also want to help you perform at your best when applying for a role with us. If you require any adjustments or support during the application process, please let the recruitment team know. This information will be handled with care and will not affect the outcome of your application. Ipsen is an equal opportunity employer that strictly prohibits unlawful discrimination. We recruit, employ, train, compensate, and promote without regard to an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.