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Internship Real World Evidence Rwe Jobs in Germantown, MD

AstraZeneca

Medical Lead - US Oncology

Gaithersburg, MD · On-site

... RWE (Real World Evidence) Projects across asset and tumor areas Provide additional training to enhance Field Medical team scientific acumen in collaboration with Global Medical and implement the ...

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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 May 28, 2026, the average hourly pay for internship real world evidence rwe in Germantown, MD is $15.71, according to ZipRecruiter salary data. Most workers in this role earn between $12.64 and $17.74 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, and why are they important?

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 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 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 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 popular job titles related to Internship Real World Evidence Rwe jobs in Germantown, MD? For Internship Real World Evidence Rwe jobs in Germantown, MD, the most frequently searched job titles are:
What job categories do people searching Internship Real World Evidence Rwe jobs in Germantown, MD look for? The top searched job categories for Internship Real World Evidence Rwe jobs in Germantown, MD are:
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Internship Real World Evidence Rwe jobs near you
Global Medical Affairs Leader COPD Omnichannel Confidence and Advocacy

Global Medical Affairs Leader COPD Omnichannel Confidence and Advocacy

AstraZeneca

Gaithersburg, MD • On-site

Full-time

Posted yesterday

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 70 rated pharmaceutical

Job description

The Global Medical Affairs Leader (GMAL) reports directly to the Medical Head of Inhaled COPD and plays a vital strategic business role. As an experienced leader in Medical Affairs, this individual is responsible for developing medical and promotional advocacy activities for our COPD products.

The GMAL's influence extends globally across AstraZeneca, participating in the Global Medical Team and the Global CFT team, and collaborating with medical personnel in key markets and regions. The Global Medical Affairs Lead (GMAL) for Breztri/Trixeo will shape and execute the global medical strategy. This role will drive medical confidence and advocacy, support country-level guideline pull-through and GDMT acceleration, lead the Next-Generation Product (NGP) Breztri transition and orchestrate omnichannel and AI-enabled initiatives.

Essential Job Responsibilities:

  • Medical Strategy and Leadership: Provide global oversight of medical affairs for Breztri/Trixeo, ensuring strategic alignment with therapeutic priorities, lifecycle management, commercial objectives, and scientific standards.

  • Medical Confidence and Advocacy Initiatives: Establish external credibility by disseminating robust evidence, engaging thought leaders, and facilitating scientific dialogue; design and implement advocacy initiatives with key stakeholders to reinforce Breztri's clinical value proposition.

  • Guideline and GDMT Support: Collaborate with country medical teams to support the adoption and execution of guideline-driven initiatives and accelerate GDMT (Guideline-Directed Medical Therapy) implementation; supply scientifically validated resources and frameworks to ensure consistency with local healthcare practices.

  • NGP Breztri Transition: Manage cross-regional planning and execution of the NGP transition throughout the EU, while preparing for upcoming launches. Coordinate integrated evidence generation, anticipate label changes as needed, and deliver comprehensive education for healthcare professionals to optimize launch and post-launch impact.

  • Global-to-Local Enablement: Develop consistent global medical narratives, educational platforms, and toolkits; mentor and align regional and country medical teams on execution standards and key performance indicators.

  • Medical Governance and Compliance: Maintain rigorous scientific integrity, uphold ethical standards, and ensure compliance across medical activities, including both promotional and non-promotional reviews.

  • Cross-Functional Collaboration: Work collaboratively with R&D, Commercial, Market Access, Regulatory, Safety, and Digital/Analytics to achieve integrated planning, seamless execution, and continuous improvement informed by market insights.

  • Insights and Performance Management: Define measurable goals, create dashboards, and establish learning agendas for priority markets; utilize AI and analytics to generate actionable insights and refine the global medical advocacy approach

Essential for the role:

  • Demonstrate in-market or regional medical affairs expertise in Respiratory, translating scientific evidence and market dynamics into actionable medical strategies and advocacy roadmaps tailored to local needs; successfully led advocacy initiatives in a local context.

  • Build and maintain effective relationships with key external experts (KEEs), patient advocacy groups, healthcare organizations, payers, and healthcare systems, resulting in collaborative initiatives and improved patient outcomes.

  • Demonstrated ability to build internal and external networks across geographies and cultures, developing and implementing confidence and advocacy strategies in a global context.

  • Generate and analyze substantial clinical and real-world evidence, including successful leadership of Phase 2, 3, or 4 clinical trials, and driving impactful RWE projects such as world-class registries and label-enhancing data initiatives.

  • Cultivate strong working relationships with global thought leaders, key experts, professional societies, and other healthcare organizations, contributing to high-impact collaborations and industry advancement.

  • Communicate complex scientific concepts clearly and effectively, delivering impactful presentations and ensuring high-quality, objective data communication.

Desirable for the role:

  • Doctoral level degree: MD, PhD, or PharmD

  • Expertise in advocacy activities, sustainability and next-generation propellants is desirable

  • Relevant experience beyond Medical Affairs (e.g. in a marketing/R&D/Market Access/ CI role) is a nice to have.

  • Experience launching new products or indications, and in developing and launching medicines in key geographies (e.g. US, China, Japan)

  • Expertise in clinical and implementation research

Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Apply today.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We follow all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

The annual base pay for this position ranges from $193,281 - 289,922. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus

Date Posted

02-Apr-2026

Closing Date

28-May-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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