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Internship Real World Evidence Rwe Jobs in Germantown, MD

This position requires highly motivated problem solvers with a strong track record in real-world evidence generation and scientific publications, advanced methodological and analytical skills, strong ...

This role defines and drives the statistical strategy for programs from early development through pivotal trials and regulatory submission - and in the future will drive real-world evidence ...

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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:
What cities near Germantown, MD are hiring for Internship Real World Evidence Rwe jobs? Cities near Germantown, MD with the most Internship Real World Evidence Rwe job openings:
Director, BPM Evidence Publications CVRM

Director, BPM Evidence Publications CVRM

AstraZeneca

Gaithersburg, MD • On-site

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


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

Main Duties and Responsibilities The Director, BPM Evidence Publications CVRM (Publications Lead) has direct accountability for the development and execution of strategic publication plans for global clinical registration studies (R&D) and non-clinical trial sources including HEOR, epidemiology, real-world evidence (RWE), payer, and non-interventional studies. The role drives timely, high-quality and compliant scientific communications by combining deep publications strategy and therapy-area expertise with the responsible use of advanced analytics and AI-enabled tool. As part of this role, the Publications Lead engages and collaborates with internal colleagues and external experts, investigators, journals, conference organizers and external bodies to deliver strategic publication and communication activities.

The role also collaborates effectively with regional and country affiliates to develop and maintain integrated external scientific communications plans for regional and local healthcare professionals, payers, and patients. The Publications Lead is further responsible for ensuring ethical compliance with AZ standards and external publication guidelines of the publications plans and deliverables, and they ensure that all publications represent transparent and fair-balanced communications that enhance the Company's external scientific reputation. Essential Requirements Minimum of a Bachelor's Degree in a scientific discipline with research experience with Minimum 5 years of experience Demonstrated experience in the publications field, or medical communications gained through working in the pharmaceutical industry or a medical communications agency.

Demonstrated project management experience. Broad understanding of drug development process. Working knowledge of AI/LLM concepts relevant to scientific publishing.

Demonstrated performance, budget, and resource management skills in a global organization Excellent leadership and project management skills to deliver in a complex multidisciplinary environment. Ability to establish and maintain professional relationships with external experts, investigators, journal editors and publishers and professional bodies. Ability to effectively manage multiple stakeholders and projects to within budget.

Flexibility and adaptability to manage long-term activities in a constantly changing internal and external environment. Desirable Requirements Relevant post-graduate degree. Experience of working globally, cross-culturally and cross-functionally.

Proven experience designing and scaling AI-enabled workflow (e.g. prompt libraries, fine-tuning/evaluating LLMs), with measurable impact, e.g. timelines

CMPP Certification. Working knowledge of iEnvision publication management system, and Microsoft Office products. Strong therapeutic knowledge in cardiovascular, renal and / or metabolic therapy areas, with proven ability to adapt quickly to other therapeutic specialties.

The annual base pay for this position ranges from 193,281.60 - 289,922.40 USD Annual (80% - 120%). 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 opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.

If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. When we put unexpected teams in the same room, we unleash bold thinking with the power toinspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions.

That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility.

Join us in our unique and ambitious world. At AstraZeneca, work is driven by a clear purpose: bending the global mortality curve by bringing life-changing medicines to patients faster, shaping the future by spotting scientifically led opportunities and rapidly scaling them across the healthcare ecosystem. Teams combine deep scientific expertise with commercial insight to design evidence strategies that improve outcomes across the whole patient journey - from clinical trials through to real-world care - in an environment that values autonomy, experimentation, learning from failure and diverse perspectives.

Here there is energy, pace and a strong sense of impact: collaborating with top talent across disciplines opens up countless opportunities to grow skills, build a varied career path and develop as a future leader while contributing to meaningful change in cardiovascular, renal, metabolic and other disease areas. Ready to help define how evidence publications can transform patient outcomes worldwide. Apply now.

Date Posted 20-May-2026 Closing Date 02-Jun-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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