The Senior Director, HEOR/RWE is responsible for developing the strategy and executing HEOR plans and activities related to all Revolution Medicines assets intended for use in non-small cell lung ...
The Senior Director, HEOR/RWE is responsible for developing the strategy and executing HEOR plans and activities related to all Revolution Medicines assets intended for use in non-small cell lung ...
The Senior Director, HEOR/RWE is responsible for developing the strategy and executing HEOR plans and activities related to all Revolution Medicines assets intended for use in non-small cell lung ...
The Senior Director, HEOR/RWE is responsible for developing the strategy and executing HEOR plans and activities related to all Revolution Medicines assets intended for use in non-small cell lung ...
Sr Engineer I, Electrical Projects
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RWE Americas, LLC To start as soon as possible, full time, permanent Functional area: Engineering Remuneration: Exempt The Sr Engineer I, Electrical Projects , is responsible for overseeing the ...
Sr Engineer I, Electrical Projects
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Business Development Manager West
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State Government Affairs Director
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State Government Affairs Director
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Sr Project & Operations Communications Manager
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Sr Project & Operations Communications Manager
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Rwe information
See California salary details
$96K - $107.7K
4% of jobs
$107.7K - $119.5K
9% of jobs
$119.5K - $131.2K
10% of jobs
$132K is the 25th percentile. Wages below this are outliers.
$131.2K - $143K
17% of jobs
The median wage is $151.8K / yr.
$143K - $154.7K
13% of jobs
$154.7K - $166.5K
15% of jobs
$173.9K is the 75th percentile. Wages above this are outliers.
$166.5K - $178.2K
11% of jobs
$178.2K - $190K
8% of jobs
$190K - $201.7K
6% of jobs
$201.7K - $213.5K
3% of jobs
$213.5K - $225.2K
3% of jobs
$96K
$157.4K
$225.2K
How much do rwe jobs pay per year?
What is an RWE?
An RWE (Real-World Evidence) job involves analyzing real-world data from sources like electronic health records, claims databases, and patient registries to generate insights on treatment effectiveness, safety, and healthcare outcomes. Professionals in this field work in pharmaceuticals, healthcare, and regulatory organizations to support clinical decision-making and policy development. Their role includes data analysis, study design, and interpretation of findings to inform medical practice and drug development.
What are the primary day-to-day responsibilities of an RWE specialist?
As an RWE specialist, your daily tasks typically include designing and conducting observational studies using healthcare databases or patient registries, analyzing real-world data, and generating actionable insights for clinical or commercial teams. You may also collaborate closely with epidemiologists, medical writers, and regulatory affairs professionals to ensure the quality and compliance of research outputs. RWE specialists frequently present study results to both internal stakeholders and external partners, translating complex data into clear, actionable recommendations. The role offers the opportunity to work on diverse therapeutic areas and contribute valuable evidence supporting real-world patient outcomes.
What are the key skills and qualifications needed to thrive in the RWE position, and why are they important?
To thrive as a Real World Evidence (RWE) specialist, you need a solid background in epidemiology, biostatistics, and data analysis, typically supported by a relevant degree in life sciences or public health. Familiarity with data analysis software (such as SAS, R, or Python), database management systems, and knowledge of healthcare data standards are usually required. Critical thinking, attention to detail, and effective communication skills are vital soft skills for interpreting complex data and collaborating across multidisciplinary teams. These abilities are essential for accurately generating insights from real-world data to inform patient outcomes, regulatory decisions, and healthcare strategies.

Full-time
Posted 26 days ago
Job description
The Opportunity:
The Senior Director, HEOR/RWE is responsible for developing the strategy and executing HEOR plans and activities related to all Revolution Medicines assets intended for use in non-small cell lung cancer (NSCLC). They will be accountable for demonstrating the value of Revolution Medicines products to healthcare organizations, allowing them to make informed decisions. They will work closely with the Medical Affairs team as well as other cross-functional teams to optimize the Integrated Evidence Plan (IEP) and to deliver evidence supporting the use of Revolution Medicines products. The candidate must also be able to provide input and strategic guidance on the global value of the product as well as have demonstrated success in evidence generation globally. The Senior Director HEOR/RWE will participate with the matrix team across the function to ensure alignment of all activities with the strategic and tactical plans. This is an exceptional opportunity to contribute to the advancement of healthcare by providing evidence that can shape the future of patient care in oncology.
Reporting to the Executive Director of HEOR/RWE Lung, the Senior Director, HEOR/RWE :
Align with Medical Affairs and Development leadership to design research and deliver evidence consistent with the medical strategy and IEP.
Develops and evolves product HEOR/RWE strategy globally, including integration with development, commercial, regulatory, and market access planning.
Deliver HEOR/RWE tactics with quality and in alignment with agreed upon timing.
Provide HEOR/RWE leadership on matrix teams and working groups.
Work with the HEOR/RWE and Medical Affairs leadership to ensure critical value insights are communicated to key internal teams.
Provide HEOR evidence which addresses the needs and expectations of key stakeholders such as patients, healthcare providers, payers and Health Technology Assessment (HTA) agencies.
Leads enterprise partnerships with payers, HTA agencies, and global consortia to help shape access strategy, policies, evidence standards, and evidence generation activities.
Effectively present research findings to internal and external stakeholders to improve internal decision making and to promote wider adoption of research findings across external stakeholders.
Facilitate the communication of the value proposition of Revolution Medicines' portfolio, allowing key healthcare and formulary professionals to make informed therapeutic decisions.
Engage and collaborate with external partners including payers, health care providers, thought leaders, patient advocates, and decision-makers to establish/maintain strong partnerships and gather insights into research programs.
Facilitate and implement real-world research partnership engagements with leading healthcare, academic and payer organizations to co-create value evidence and help drive evidence-based optimal care.
Stay up to date with and add to the advancements in health economics methodologies and best practices.
Identify and interface with HEOR & RWE experts and organizations, profile data sources and related organizations as they relate to Revolution Medicines' portfolio and therapeutic areas.
Closely monitor new trends in health policy and payer environment, assess competitive data gaps and communicate to the organization, to help Revolution Medicines build industry-leading capabilities and be on the cutting edge of evidence-based medicine and HEOR research.
Required Skills, Experience and Education:
Deep expertise in health economics, outcomes research, patient-reported outcomes or related fields in the biotechnology or pharmaceutical industry.
Experience in oncology HEOR and RWE development.
Track record of high impact publications in HEOR/RWE topics.
Strong written and interpersonal communication skills, with an ability to present complex technical information clearly.
Knowledge and experience in managed care, integrated delivery networks, formulary decision-making, and payment/access models.
Ability to establish relationships with experts in real world evidence (RWE) and therapeutic areas of interest.
Preferred Skills:
12+ years of relevant experience in the pharmaceutical/biotech industry.
Global launch experience.
Experience related to NSCLC.
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