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Internship Real World Evidence Rwe Jobs in Kentucky

Servier

Associate Director, HEOR & RWE

Boston, KY · On-site

... evidence readiness, ensuring that robust health economic models, AMCP dossiers, and real-world ... Design and execute innovative RWE solutions, such as external control arms, to provide essential ...

Houston Dose

$134K - $176K/yr

Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g ...

Osmind

$110K - $125K/yr

Turn primary research and real-world evidence into insights that move a commercial project forward Data and evidence * Analyze real-world datasets spanning claims and EHR data to find actionable ...

Celldex Therapeutics, Inc.

Responsibilities Epidemiology & Real-World Evidence Strategies * Develop and execute epidemiology and real-world evidence strategies aligned to clinical development, regulatory, safety, Medical ...

Servier

Sr Medical Director (Heme Oncology)

Boston, KY · On-site

Integrate clinical insights, health economics, and real-world evidence (RWE) to build a cohesive medical platform that addresses unmet patient needs and demonstrates product value. * Allocate and ...

Servier

Sr Medical Director (Heme Oncology)

Boston, KY · On-site

Integrate clinical insights, health economics, and real-world evidence (RWE) to build a cohesive medical platform that addresses unmet patient needs and demonstrates product value. * Allocate and ...

MSD Malaysia

$39K - $111K/yr

Conducting data analysis in real-world health data sources to understand data quality, disease ... In addition, the interns will attend departmental and project team meetings to gain a broad ...

Rancho BioSciences, LLC

Familiarity with emerging technologies in R&D, including AI/ML in drug discovery, real-world evidence (RWE), and digital clinical trials * Experience with data platform design (Snowflake, Databricks ...

RXinsider LTD.

Synthesize published literature, real-world evidence, internal research findings, and behavioral science frameworks into clear, business-relevant insights. Translate complex behavioral, psychosocial ...

Natus Medical Incorporated

Validate workflows, generate real-world evidence, and refine clinical use cases; translate learnings into scalable adoption models Market Intelligence & Competitive Clinical Strategy * Analyse ...

St. Jude Children's Research Hospital

Causal Inference, External Controls, and Real-World Evidence Development of principled approaches for incorporating external information into clinical trials when concurrent randomized control groups ...

Neara

Position our Real World Data solutions, spanning longitudinal outcomes intelligence, biomarker and population insights, and post-market evidence generation, with Medical Affairs and Precision ...

Novellia

... and VP-level RWE, Medical Affairs, and outcomes research leaders, and converting those ... Novellia sells real-world patient data and evidence generation to pharma and biotech. Our patients ...

Otsuka Pharmaceutical Co., Ltd

This individual develops data that demonstrate the value and real-world impact of products for ... RWE and produce data and tools * Work with payers and other appropriate organizations to uncover ...

Rutgers University

$80K/yr

Designing and supporting real world studies focused on patient outcomes, burden of illness, clinical and health economics, and policy relevant evidence * Conducting literature reviews, database ...

Veradigm Inc.

$163K - $216K/yr

Partner with RWE Consulting, Data Partnerships, Client Success, and A/R to ensure seamless delivery ... Maintain deep knowledge of Veradigm Real World Evidence solutions and data offerings and the ...

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Internship Real World Evidence Rwe information

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

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

What are popular job titles related to Internship Real World Evidence Rwe jobs in Kentucky?

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

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Cities in Kentucky with the most Internship Real World Evidence Rwe job openings:

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Infographic showing various Internship Real World Evidence Rwe job openings in Kentucky as of August 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution.

Associate Director, HEOR & RWE

Boston, KY • On-site

Servier
See more jobs at Servierexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 15 days ago

Job description

About Servier
Servier in the U.S. is a Boston-based, commercial-stage biopharmaceutical company launched by Servier Group in 2018. As a privately held organization, Servier is uniquely positioned to advance cutting-edge science, tackle underserved therapeutic areas and make patients the focus of every strategic decision.
Role Summary
The Associate Director, HEOR/RWE (Emi-Le and Solid Tumor Pipeline), is a key member of the HEOR and Scientific Communication team within the US Medical Affairs organization. This individual is responsible for the strategic development and execution of early evidence generation initiatives for Servier's oncology programs, including Emi-Le (e.g., ACC), DAY301 and additional pipelines.
The primary focus of this role is to identify and address unmet medical needs, access barriers, and value gaps prior to launch. The Associate Director will spearhead the development of Patient-Reported Outcome (PRO) strategies to capture the patient voice and design innovative RWE solutions, such as external control arms to contextualize clinical data from single-arm trials. Furthermore, this individual is responsible for driving launch evidence readiness, ensuring that robust health economic models, AMCP dossiers, and real-world datasets are developed in time to support successful launch. By partnering closely with Clinical Development, Translational Science, and US Medical/Access teams, this individual ensures that the early evidence base robustly supports future value demonstration and reimbursement pathways for these high-priority pipeline assets.
Primary Responsibilities
Key Responsibilities: Associate Director
  • Strategic Leadership & Planning:
    • Lead the development of comprehensive evidence strategy (e.g., economic, comparative effectiveness) and operational plans for pipeline assets, with a focus on establishing early value propositions for Emi-Le (ACC).
    • Identify and address unmet medical needs and access barriers in collaboration with cross functional teams to enable development of robust health economic and value narratives.
    • Collaborate with clinical development teams to design and incorporate PRO measures within early-phase clinical trials, serving as a Subject Matter Expert (SME) for engagements with regulatory and payer bodies.
    • Provide scientific support to facilitate early market access planning and preparatory payer engagements for the pipeline portfolio.
    • Maintain an up-to-date awareness of the industry's regulatory, payer, and policy landscape, particularly regarding the use of RWE and PROs in oncology and assess its potential impact on evidence generation.
    • Mentor junior team members and contribute to a culture of learning, integrity, and innovation within the Value, Evidence, and Communication function.
  • Evidence Generation and Impact Measurement:
    • Oversee the end-to-end delivery of RWE studies (e.g., database analysis, chart reviews, prospective registries) to characterize unmet needs and disease burden in niche solid tumor indications.
    • Design and execute innovative RWE solutions, such as external control arms, to provide essential comparative context for clinical data derived from single-arm trials.
    • Deliver "launch-ready" U.S. economic models and AMCP dossiers to optimize patient access and reimbursement ahead of commercial market entry.
    • Ensure all research initiatives strictly adhere to internal study governance processes, ensuring high ethical and scientific standards, including obtaining necessary internal approvals and cross-functional alignment.
    • Work with external vendors and internal teams to design and execute pipeline oncology evidence projects, ensuring timely and quality delivery while managing budgets and CRO performance.
    • Ensure timely measurement and communication of the external and internal impact of generated evidence to demonstrate value to the organization.
    • Translate research outputs into practical tools (e.g., value decks, proactive/reactive field materials) in collaboration with the scientific communications team, equipping field medical and access teams for future launches.
  • Alliance Management & Global Collaboration:
    • Coordinate with Servier Global counterparts to ensure US pipeline evidence generation strategies (e.g., PRO selection, RWE design) complement and support global value narratives.
    • Manage the collaborative review of evidence generation plans within joint alliance frameworks to ensure consistency in the global value story for pipeline assets.
  • Communication & Stakeholder Engagement:
    • Lead communication with Medical Affairs and other functional leadership on planned and ongoing pipeline research initiatives, key findings, and their strategic impact.
    • Drive pull-through and communication of evidence strategy to internal and external stakeholders, including cross-functional asset and governance teams, healthcare decision-makers, and clinical practitioners.
    • In collaboration with the Patient Advocacy team, champion the "Patient Voice" by effectively communicating the results of PRO strategies and unmet need studies to internal and external experts to shape the perceived value of the pipeline.

Education and Required Skills: Associate Director
  • Advanced degree (PhD, PharmD, MS) in Health Outcomes, Pharmacoeconomics, Epidemiology, or a related field, with relevant experience in oncology.
  • 6+ years of experience in the pharmaceutical or healthcare industry, specifically within a Value, Evidence, and Communication function (or equivalent HEOR, RWE, Medical Evidence Generation), with proven experience in early-stage pipeline evidence strategy development and execution.
  • Deep expertise in innovative RWE methodologies required for pipeline assets, including the design of external/synthetic control arms to contextualize single-arm clinical trials and the characterization of unmet medical needs in rare oncology indications.
  • Strong knowledge of the U.S. regulatory framework and payer landscape, with specific experience designing and implementing evidence strategies (e.g., natural history studies, PRO selection) that meet both payer and regulatory requirements for novel therapies.
  • Advanced technical expertise in outcomes research, economic modelling, and PRO research, coupled with excellent communication skills to effectively convey complex scientific data to varied audiences.
  • Proven track record in driving "launch evidence readiness," including the development of AMCP dossiers, value stories, and economic models tailored for initial market entry.
  • Strong project management capabilities and the ability to work effectively in a matrix organization, ensuring adherence to internal study governance and scientific standards.
  • Effective in communicating research findings and able to translate these into actionable insights and compelling value narratives for diverse internal and external stakeholders.
  • Proven ability to manage complex projects, alliance partnerships, and cross-functional initiatives with strategic agility and attention to detail.
  • Collaborative leadership style with a track record of working across teams, functions, and geographies to drive functional excellence.
  • High emotional intelligence, with the ability to lead through influence, resolve challenges, and build consensus in a matrixed organization, particularly when managing the evolving data sets of pipeline assets.

Travel and Location
  • Boston Based, hybrid role reporting to the Seaport office 2-3x per week
  • 15-20% Travel

Job Description
Candidate Profile
Servier's Commitment
Servier is committed to modeling diversity, equity, and inclusion within the industry. We are dedicated to fostering an environment that maintains equitable treatment for all and we welcome applicants who are passionate, committed, and innovative individuals. We encourage candidates to apply to our open roles as we are always willing to consider experiences and skills beyond what is listed in the job description.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Salary Range
The salary range for this role is $184,000 - $218,000. An employee's pay position within the salary range will be based on several factors including, but not limited to, relevant education, qualifications, certifications, experience, skills, geographic location, performance, and business or organizational needs. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Employees in this position are also eligible for Short-Term and Long-Term incentive programs. Servier also offers a competitive and comprehensive benefits package that includes benefits such as medical, dental, vision, flexible time off (Servier provides unlimited sick time and flex time, and does not accrue time off), 401(k), life and disability insurance, recognition programs among other great benefits (all benefits are subject to eligibility requirements). For more information on our benefits, please visit this link.

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