Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Director, BPM Evidence Publications CVRM
Gaithersburg, MD · On-site
$164 - $247/hr
... real-world evidence (RWE), payer, and non-interventional studies.The role drivestimely,high-qualityand compliant scientific communications by combining deeppublications strategy andtherapy ...
New
Director, BPM Evidence Publications CVRM
Gaithersburg, MD · On-site
$164 - $247/hr
... real-world evidence (RWE), payer, and non-interventional studies.The role drivestimely,high-qualityand compliant scientific communications by combining deeppublications strategy andtherapy ...
New
Senior Global Medical Affairs Leader, CardioRenal
Gaithersburg, MD · On-site
$244 - $365/hr
Senior GMALs own the evidence generation strategy--demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior Global Medical Affairs Leader, CardioRenal
Gaithersburg, MD · On-site
$244 - $365/hr
Senior GMALs own the evidence generation strategy--demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and ...
Ensuring clinical trial designs, biostatistics, and real-world evidence (RWE) comply with human subject protection standards and safety regulations before devices reach the market. Key Duties and ...
Quick apply
Ensuring clinical trial designs, biostatistics, and real-world evidence (RWE) comply with human subject protection standards and safety regulations before devices reach the market. Key Duties and ...
Ensuring clinical trial designs, biostatistics, and real-world evidence (RWE) comply with human subject protection standards and safety regulations before devices reach the market. Key Duties and ...
Ensuring clinical trial designs, biostatistics, and real-world evidence (RWE) comply with human subject protection standards and safety regulations before devices reach the market. Key Duties and ...
Principal Contracts Manager - Hybrid
Bethesda, MD · On-site
$144K/yr
Experience supporting contracts for clinical research, biomedical research, real-world data (RWD), real-world evidence (RWE), health informatics, and public health programs on behalf of NIH, HHS, CDC ...
Principal Contracts Manager - Hybrid
Bethesda, MD · On-site
$144K/yr
Experience supporting contracts for clinical research, biomedical research, real-world data (RWD), real-world evidence (RWE), health informatics, and public health programs on behalf of NIH, HHS, CDC ...
Principal Contracts Manager - Hybrid
Bethesda, MD · Hybrid
$95K - $127K/yr
Experience supporting contracts for clinical research, biomedical research, real-world data (RWD), real-world evidence (RWE), health informatics, and public health programs on behalf of NIH, HHS, CDC ...
Principal Contracts Manager - Hybrid
Bethesda, MD · Hybrid
$95K - $127K/yr
Experience supporting contracts for clinical research, biomedical research, real-world data (RWD), real-world evidence (RWE), health informatics, and public health programs on behalf of NIH, HHS, CDC ...
Director, Global Oncology Publications
Gaithersburg, MD · On-site
$193K - $289K/yr
... real-world evidence (RWE), payer, and non-interventional studies. * Head the development of scientific, clinical and RWE planning data intotimelypublications for prescribers, payers, and patients ...
Director, Global Oncology Publications
Gaithersburg, MD · On-site
$193K - $289K/yr
... real-world evidence (RWE), payer, and non-interventional studies. * Head the development of scientific, clinical and RWE planning data intotimelypublications for prescribers, payers, and patients ...
Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g ...
Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g ...
At the heart of our mission is our patented Topical Wound Oxygen (TWO2) therapy, the only device of its kind proven effective in both Randomized Controlled Trials (RCTs) and Real-World Evidence (RWE ...
At the heart of our mission is our patented Topical Wound Oxygen (TWO2) therapy, the only device of its kind proven effective in both Randomized Controlled Trials (RCTs) and Real-World Evidence (RWE ...
Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g ...
Medical Affairs (including Medical Directors), Real-World Evidence (RWE), Clinical Development/Operations, Medical Information, Compliance/Legal, and cross-functional commercial colleagues (e.g ...
Data Scientist-HEOR
Washington, DC · On-site +1
$90K - $140K/yr
This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...
Data Scientist-HEOR
Washington, DC · On-site +1
$90K - $140K/yr
This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...
Data Scientist-HEOR
Washington, DC · On-site
$90K - $140K/yr
This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...
Quick apply
Data Scientist-HEOR
Washington, DC · On-site
$90K - $140K/yr
This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...
Data Scientist-HEOR
Washington, DC · On-site
$90K - $140K/yr
This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...
Data Scientist-HEOR
Washington, DC · On-site
$90K - $140K/yr
This position offers the opportunity to apply your analytical expertise to real-world evidence (RWE), health outcomes, and market access challenges while making a measurable impact on how treatments ...
... real-world evidence (RWE), payer, and non-interventional studies. Head the development of scientific, clinical and RWE planning data into timely publications for prescribers, payers, and patients ...
... real-world evidence (RWE), payer, and non-interventional studies. Head the development of scientific, clinical and RWE planning data into timely publications for prescribers, payers, and patients ...
... real-world evidence (RWE), payer, and non-interventional studies. * Head the development of scientific, clinical and RWE planning data into timely publications for prescribers, payers, and patients ...
... real-world evidence (RWE), payer, and non-interventional studies. * Head the development of scientific, clinical and RWE planning data into timely publications for prescribers, payers, and patients ...
Director, Value Strategy, US Market Access
Gaithersburg, MD · On-site
$186 - $279/hr
She/he will be responsible for synthesizing clinical trial data, real world evidence, and ... Analyzing RCT/RWE/HEOR & other data * Writing protocols for data extraction and synthesis
Director, Value Strategy, US Market Access
Gaithersburg, MD · On-site
$186 - $279/hr
She/he will be responsible for synthesizing clinical trial data, real world evidence, and ... Analyzing RCT/RWE/HEOR & other data * Writing protocols for data extraction and synthesis
Real World Evidence Rwe information
What is real world evidence (RWE)?
How does a real world evidence (RWE) professional collaborate with cross-functional teams?
What are the key skills and qualifications needed to thrive as a real world evidence (RWE) professional?
What is the difference between Real World Evidence Rwe vs Clinical Data Analyst?
| Aspect | Real World Evidence Rwe | Clinical Data Analyst |
|---|---|---|
| Required credentials | Typically requires a background in healthcare, epidemiology, or biostatistics, often with a master's or PhD | Usually requires a degree in health informatics, biostatistics, or related fields, with similar certifications |
| Work environment | Primarily in healthcare, pharmaceutical, or research organizations analyzing real-world data | In clinical research settings, hospitals, or pharmaceutical companies analyzing clinical trial data |
| Employer and industry usage | Used by pharma companies, healthcare providers, and research institutions to generate real-world insights | Used 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 are popular job titles related to Real World Evidence Rwe jobs in Washington?
For Real World Evidence Rwe jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Real World Evidence Rwe jobs in Washington look for?
The top searched job categories for Real World Evidence Rwe jobs in Washington are:
What cities in Washington are hiring for Real World Evidence Rwe jobs?
Cities in Washington with the most Real World Evidence Rwe job openings:

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 16 days ago
Key responsibilities
Develops and leads global medical strategies within the CVRM therapy area.
Guides cross-functional and cross-regional teams to deliver and exceed medical goals.
Shapes global medical agendas through leadership of medical teams, product teams, and disease area teams.
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
23rd of 86 rated pharmaceutical
Job description
Job is based either in Gaithersburg, MD or Boston, MA and requires to be in the office 3 days a week.
Role Summary:
Reporting to the Medical Head the Senior Global Medial Affairs Lead Cardiovascular is a highly experienced Medical Affairs leader with proven vision and impact. This individual develops and leads bold medical strategies within the CVRMtherapy area, expertly guiding cross-functional and cross-regional teams to deliver and exceed ambitious goals. The Senior GMAL's influence is enterprise-wide-shaping global medical agendas through Global Medical Team, Global Product Team, and Disease Area Team leadership, and deep partnership with Medical and Commercial functions in markets and regions worldwide.
This role demands a leader who champions innovative, disruptive thinking-identifies and shapes breakthrough opportunities, reimagines market dynamics, and accelerates high-impact evidence generation and medical change initiatives. The Senior GMAL navigates and transforms health systems, leverages digital and advanced analytics, drives stakeholder engagement, and ensures AstraZeneca's science leads externally and internally through world-class medical evidence and strategic partnerships.
Expectations of a Senior GMAL include:
Strategy & Transformation:The Senior GMAL designs and leads the implementation of product and disease area strategies, as well as ambitious practice change initiatives, at a global level. This requires a deep understanding of healthcare system pathways, regulatory landscapes, market access, and competitive dynamics. The Senior GMAL consistently delivers innovative, disruptive solutions to shape markets, challenges status quo thinking, and uses digital proficiency to identify data-driven opportunities, preparing for launch and life cycle management.
Medical Evidence Leadership:Senior GMALs own the evidence generation strategy-demonstrating advanced experience in clinical research, interventional trials (Phases 2-4), and real-world evidence (RWE) programs. They shape and drive groundbreaking clinical trials, registries, and RWE studies aligned with brand, access, and practice-changing objectives. They guide the optimisation, communication, and strategic roll-out of data across scientific platforms, ensuring AstraZeneca delivers differentiated evidence that supports the needs of regulatory, payer, and healthcare providers. Clinical research, patient outcomes expertise, and deep understanding of treatment protocols underpin their ability to address evolving evidence requirements.
Advanced Scientific & Digital Engagement:The Senior GMAL blends scientific expertise with strong digital acumen. They leverage digital health tools, advanced analytics, and data platforms to transform evidence communication, personalize stakeholder engagement, and enhance patient outcomes. They are the voice of medical-crafting compelling narratives, driving digital dissemination of evidence, and ensuring accurate, impactful, and compliant scientific communications.
Guiding and Influencing Stakeholders:With significant expertise in internal and external engagement, the Senior GMAL builds and sustains powerful relationships across the healthcare ecosystem-including global and regional KOLs, professional societies, regulators, payers, patient organizations, digital innovators, and health systems. Their credibility and influence enable them to mobilize support for medical strategy, evidence generation, and healthcare change initiatives. They mentor and guide cross-functional teams, championing scientific leadership and strategic collaboration.
Regulatory Insight & Compliance:The Senior GMAL possesses keen regulatory understanding and ensures clinical trial and evidence generation initiatives are designed for both scientific and regulatory success. They anticipate evolving regulatory and payer requirements for evidence, ensuring high quality, compliant data generation and communication at every stage.
Essential for the role:
Minimum of Master's degree or higherwith at least5 yearsof experience in the pharmaceutical industry (Medical, Marketing, R&D, Market Access), or extensive experience within a health system (clinical, pharmacy, pathway design, etc.).
Demonstrated leadership in complex, global healthcare environments, including leading franchise/TA business in key markets, driving brand performance, and managing large, diverse teams including global launch of major products.
Significant expertise and strategic insight into healthcare system pathways, regulatory landscapes, market-shaping, and external stakeholder engagement.
Strong track record of internal and external network building, collaboration across geographies and matrix teams, and effective mentoring of junior colleagues or peers.
Digital proficiency, leveraging digital health tools and data platforms to advance evidence generation and communication.
Deep understanding of patient care pathways, evolving treatment protocols, scientific literature, and contemporary approaches to healthcare transformation.
Proven ability to guide, influence, and align diverse stakeholders-including thought leaders, regulatory bodies, patient groups, and payer organisations.
Desirable for the role:
Doctoral-level degree (MD, PhD, PharmD) in a relevant discipline.
Recognized expertise in the relevant or related therapeutic area, often evidenced by a history of clinical practice, research leadership, or significant external engagement.
Advanced experience designing, leading, and interpreting clinical research programs, including pivotal clinical trials (Ph2-Ph4), practice-changing RWE studies, and implementation of innovative evidence generation approaches.
Broad experience beyond Medical Affairs; for example, prior roles in Marketing, R&D, or Market Access.
Long-standing relationships with global KOLs, societies, regulators, digital health partners, and innovative healthcare organisations.
Track record of launching new products or indications in multiple, diverse markets (e.g., US, China, EU), and successfully developing and executing global medical strategies.
The annual base payfor this position ranges from $243,569 - 365,379 . 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.
Date Posted
21-Aug-2026Closing Date
24-Sep-2026Our 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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About AstraZeneca
Sourced by ZipRecruiter
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Cambridge, Cambridgeshire, GB