2

Remote Real World Evidence Rwe Jobs in Pennsylvania

... real-world evidence (RWE), pharmacoeconomics, and health outcomes to support informed formulary ... Location: Remote in the United States. Reports to: Director, HEOR. Roles and responsibilities ...

$35/hr

Opportunities Available As a Real-World Evidence Data Science intern at Stryker, you will: * Work ... Shadow cross-functional team meetings to gain exposure to how RWE informs regulatory, reimbursement ...

$35/hr

Opportunities Available As a Real-World Evidence Data Science intern at Stryker, you will: * Work ... Shadow cross-functional team meetings to gain exposure to how RWE informs regulatory, reimbursement ...

$35/hr

Opportunities Available As a Real-World Evidence Data Science intern at Stryker, you will: * Work ... Shadow cross-functional team meetings to gain exposure to how RWE informs regulatory, reimbursement ...

$35/hr

Opportunities Available As a Real-World Evidence Data Science intern at Stryker, you will: * Work ... Shadow cross-functional team meetings to gain exposure to how RWE informs regulatory, reimbursement ...

$35/hr

Opportunities Available As a Real-World Evidence Data Science intern at Stryker, you will: * Work ... Shadow cross-functional team meetings to gain exposure to how RWE informs regulatory, reimbursement ...

$35/hr

Opportunities Available As a Real-World Evidence Data Science intern at Stryker, you will: * Work ... Shadow cross-functional team meetings to gain exposure to how RWE informs regulatory, reimbursement ...

$35/hr

Opportunities Available As a Real-World Evidence Data Science intern at Stryker, you will: * Work ... Shadow cross-functional team meetings to gain exposure to how RWE informs regulatory, reimbursement ...

next page

Showing results 1-20

Remote Real World Evidence Rwe information

What is a remote real world evidence RWE professional?

Remote Real World Evidence (RWE) jobs involve gathering, analyzing, and interpreting data from real-world sources—such as electronic health records, insurance claims, patient registries, and wearable devices—to inform healthcare decisions. Professionals in these roles typically work for pharmaceutical companies, research organizations, or healthcare technology firms. Remote RWE jobs allow employees to contribute to research and data analysis from home or other off-site locations, using digital tools to collaborate with teams and stakeholders. These positions are crucial for understanding how medical treatments perform outside of controlled clinical trials, ultimately improving patient care and supporting regulatory submissions.

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

To thrive as a Remote Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, or related life sciences, typically supported by an advanced degree (e.g., MPH, MS, PhD). Familiarity with statistical software such as SAS, R, or Python, and experience working with large healthcare databases and electronic health records are crucial. Excellent analytical thinking, problem-solving abilities, and effective communication skills help translate complex data into actionable insights for stakeholders. These competencies ensure the generation of robust, real-world data analyses that inform healthcare decisions and regulatory submissions.

What are some common challenges faced by remote real world evidence RWE professionals and how can they be addressed?

Remote RWE professionals often encounter challenges such as managing large and diverse datasets, ensuring data privacy, and coordinating effectively with cross-functional teams across different time zones. To address these, it's important to have strong data management skills, familiarity with relevant regulations (like GDPR or HIPAA), and effective communication tools. Actively engaging in regular virtual meetings and leveraging collaborative platforms can help maintain alignment with stakeholders and ensure project milestones are met.

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

AspectRemote Real World Evidence RweRemote Data Analyst
Required CredentialsAdvanced degrees in healthcare, epidemiology, or biostatistics; experience with RWE methodologiesBachelor's or master's in data science, statistics, or related fields; proficiency in data analysis tools
Work EnvironmentCollaborates with healthcare providers, pharma companies, and regulatory agencies; focuses on healthcare dataWorks across industries; analyzes large datasets to inform business decisions
Industry UsagePrimarily in healthcare, pharmaceuticals, and regulatory sectorsAcross various sectors including finance, marketing, and healthcare

Remote Real World Evidence Rwe specialists focus on analyzing healthcare data to generate evidence for medical and regulatory decisions, requiring healthcare-specific knowledge. Remote Data Analysts handle diverse datasets across industries, emphasizing data processing and reporting skills. While both roles involve data analysis, RWE roles are more specialized in healthcare and regulatory contexts.

What are the most commonly searched types of Real World Evidence Rwe jobs in Pennsylvania?

The most popular types of Real World Evidence Rwe jobs in Pennsylvania are:

What are popular job titles related to Remote Real World Evidence Rwe jobs in Pennsylvania?

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

What job categories do people searching Remote Real World Evidence Rwe jobs in Pennsylvania look for?

The top searched job categories for Remote Real World Evidence Rwe jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Remote Real World Evidence Rwe jobs?

Cities in Pennsylvania with the most Remote Real World Evidence Rwe job openings:

Infographic showing various Remote Real World Evidence Rwe job openings in Pennsylvania as of September 2026, with employment types broken down into 1% Internship, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Associate Director, Global Health Economics & Outcomes Research (RWE)

Conshohocken, PA • On-site, Remote

Madrigal Pharmaceuticals Corporation
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago


Key responsibilities

  • Design, develop, and execute real-world evidence (RWE) projects and strategies to support the value demonstration of Madrigal's medicines, particularly Rezdiffra.

  • Analyze complex real-world data sources, build and maintain data warehouses, and develop analytical pipelines using R, SQL, Python, and modern platforms to generate evidence.

  • Support the design and implementation of pragmatic and implementation science studies to evaluate treatment effectiveness, care delivery, and patient outcomes in routine clinical settings.


Job description

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight against MASH.
Madrigal's medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra is the first and only medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c).
Our success is driven by our people. We are building a dynamic, inclusive, and high-performing culture that values scientific excellence, operational rigor, and collaboration. To support our continued growth, we are strengthening our workforce strategy to ensure we have the right talent, at the right time, in the right way.
The Associate Director, Global Health Economics & Outcomes Research (GHEOR), Real-World Evidence (RWE) will support the strategic goals of the GHEOR, Global Medical Affairs (GMA) and the broader business driving patient access with optimal pricing and reimbursement for Madrigal Pharmaceutical's medicines, with a focus on Rezdiffra.
This position directly impacts the ability to achieve business objectives on a global basis by providing strategic guidance and robust evidence development relevant to achieve optimal patient access by demonstrating the value of our medicines for liver health, with a primary focus on developing and deploying real-world data and evidence to support Rezdiffra and the Madrigal portfolio, in a federated operating model that includes service delivery across the enterprise.
This role will be responsible for developing and executing RWE projects and strategies against the global integrated evidence plans, including dissemination of technical deliverables related to real-word data and evidence. The role will also support the design and execution of pragmatic, prospective real-world and implementation science studies to evaluate treatment effectiveness, care delivery and adoption of evidence-based practices in routine clinical settings. Reporting to the Senior Director, GHEOR (RWE), the incumbent will be working closely with the GMA, Clinical Development & Biostatistics, Access and Commercial, Regional and in-Country teams to foster a culture that promotes innovation, optimal population health and patient centricity.
All incumbents are responsible for adhering to applicable Madrigal policies and procedures.
Key Responsibilities and Primary Activities:
Approximately 60% of this role focuses on executing functional objectives, and the remaining 40% is dedicated to providing support for strategic direction and adapting priorities to achieve organizational goals.
  • Evidence Generation and HEOR Studies
    • Analyze complex real-world data (RWD) sources such as administrative claims and electronic health records databases
    • Design, build, and maintain internal data warehouses
    • Develop and maintain reproducible analytical pipelines and real-world evidence (RWE) platforms using R programming, leveraging version control tools and collaborative coding environments (e.g., GitHub), while integrating SQL and Python where beneficial
    • Build and govern internal real-world data (RWD) analytics infrastructure by leveraging modern platforms such as Posit Workbench and Databricks to enable end-to-end RWE study execution
    • Execute both rapid analyses and full protocol-driven research studies, including retrospective observational, prospective real-world, pragmatic and implementation science studies, ensuring methodologies are robust, fit-for-purpose and scientifically sound
    • Support the design and execution of pragmatic and implementation studies that evaluate real-world treatment effectiveness, adoption of evidence-based practices, care pathways, treatment initiation, adherence and persistence, and patient outcomes in routine clinical practice
    • Leverage advanced analytic and statistical modeling techniques (e.g., Cox regression, propensity score matching, IPTW) to drive causal inference and integrate data across diverse real-world sources
    • Navigate complex datasets to leverage data that improves patient outcomes
  • Clinical and Regulatory Support
    • Ensure RWE studies adhere to FDA and EMA regulatory guidance to produce high-quality evidence supporting label expansion and HTA submissions
    • Partner with cross-functional stakeholders-including Medical Affairs, regulatory, access, clinical and data science teams-as well as external investigators and healthcare-system partners, as appropriate, to inform RWE, pragamatic and implementation research across the product lifecycle
  • Industry & Conference
    • Stay current on industry trends and advancements in RWE, HEOR, pragmatic research and implementation science methodologies
    • Present at scientific conferences and publish in key journals
  • Compliance & Quality
    • Ensure all activities comply with company SOPs, industry standards, and applicable regulations
    • Uphold the highest ethical standards in all external engagements
  • Travel Requirement
    • Travel up to 30% for scientific congress attendance, internal and external meetings
    • Ability to work across global time zones as needed

Required Qualifications, Skills & Experience:
  • Graduate degree in biostatistics, public health, epidemiology, or a similar field
  • 10-12+ years of relevant experience.
  • In-depth experience with R programming, version control and collaborative development tools (e.g., GitHub), and analytic environments such as Posit Workbench, Databricks or similar cloud-based data science platforms
  • Expertise in applying advanced statistical analytic methodologies to RWD
  • Familiarity with common commercially available RWD data assets encompassing administrative claims and EHR databases
  • Experience in delivering ad-hoc and full protocol-driven observational studies; experience with prospective real-world research, pragmatic studies, implementation science or health services research is preferred
  • Experience with liver / metabolic diseases in the RWD space would be preferred
  • A strong track record of publications
  • Strong communication skills
  • High proficiency with project management systems, Medical Affairs dashboards, CRM platforms, and enterprise collaboration tools (e.g., Veeva, Microsoft Office Suite, SharePoint, Teams, Zoom)

Preferred Attributes:
  • PhD preferred
  • Experience with SQL and Python
  • In-depth knowledge of liver disease; experience in cardiometabolic health or metabolic dysfunction-associated steatohepatitis (MASH)

Madrigal's Total Rewards strategy is based on a biotech industry peer group comparator and is inclusive of base pay, bonus and equity. Our equity offers meaningful opportunity allowing our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.
All employees receive equity, which we believe reinforces our ownership culture. Base salary is determined by several factors including the candidate's qualifications, skills, education, experience, business needs and market demands. As of the date of this posting, a good faith estimate of the current pay scale for this position, applicable to all candidates, is $184,532 - $214,918 per year. We comply with all applicable minimum wage laws.
All full-time employees receive equity, which reinforces our ownership culture and offers meaningful opportunity for our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.
Full-time employees are also eligible for comprehensive benefits, including flexible paid time off, medical, dental, vision and life/disability insurance, and 401(k) offerings (i.e., traditional, Roth, and employer match) in accordance with applicable plans. We also offer additional voluntary benefits like supplemental life insurance, legal services, and other offerings. In addition, we offer mental health benefits through our Employee Assistance Program for employees and their family. The company also provides other benefits in accordance with applicable federal, state, and local laws.
We are committed to providing reasonable accommodations for individuals with disabilities throughout the hiring process. If you need assistance, please contact HR@madrigalpharma.com.
Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or other characteristic protected by applicable federal, state, or local law.
Unsolicited resumes from agencies should not be forwarded to Madrigal. Madrigal will not be responsible for any fees arising from the use of resumes through this source. Madrigal will only pay a fee to agencies if a formal agreement between Madrigal and the agency has been established.
Applications are being accepted on an ongoing basis and can be submitted through our Madrigal Careers site.
Please be aware that we have received reports of individuals misrepresenting themselves as Madrigal Pharmaceuticals' Hiring Managers, seeking to engage with job candidates through fraudulent online advertisements or job posting sites. These unauthorized individuals are using Madrigal's name and logo in an attempt to solicit up-front fees and obtain personal information from interested job candidates. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.
Please also note that any correspondence with regard to employment would come from an authorized madrigalpharma.com email address or from an email address from one of our trusted search firm partners. We are aware that incorrect/fraudulent email addresses, with Madrigal misspelled, have been utilized in these most recent fraud attempts. If you receive unsolicited employment offers from people claiming to work for or on behalf of Madrigal, we recommend that you: do not respond to their questions; do not open any attachments; and do not click on any hyperlinks. Any questions regarding the legitimacy of job-related contacts can be directed to HR@madrigalpharma.com.