The ideal candidate is a proven commercial leader who has successfully sold Real-World Data (RWD), Real-World Evidence (RWE), analytics, SaaS, or research solutions to life sciences organizations ...
The ideal candidate is a proven commercial leader who has successfully sold Real-World Data (RWD), Real-World Evidence (RWE), analytics, SaaS, or research solutions to life sciences organizations ...
The ideal candidate is a proven commercial leader who has successfully sold Real-World Data (RWD), Real-World Evidence (RWE), analytics, SaaS, or research solutions to life sciences organizations ...
The ideal candidate is a proven commercial leader who has successfully sold Real-World Data (RWD), Real-World Evidence (RWE), analytics, SaaS, or research solutions to life sciences organizations ...
You have acquired 7+ years of experience in clinical research/development/real world evidence (RWE ); scientific study design, strong scientific background and experience with Artificial Intelligence ...
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You have acquired 7+ years of experience in clinical research/development/real world evidence (RWE ); scientific study design, strong scientific background and experience with Artificial Intelligence ...
Apply Early
Partner with Clinical Research and Medical Affairs to design real-world evidence (RWE) and outcomes studies aligned to payer and HTA expectations. * Define measurable clinical, operational, and ...
Partner with Clinical Research and Medical Affairs to design real-world evidence (RWE) and outcomes studies aligned to payer and HTA expectations. * Define measurable clinical, operational, and ...
You have acquired a minimum of 7+ years' clinical experience within FDA regulated medical device environments, with a focus on clinical research/development/real world evidence (RWE); strong ...
You have acquired a minimum of 7+ years' clinical experience within FDA regulated medical device environments, with a focus on clinical research/development/real world evidence (RWE); strong ...
Partner Research & Success Manager
Seattle, WA · On-site +1
Required Skills * 4+ years of experience working in a field which developed exposure to and understanding of real-world data (RWD), real world evidence (RWE), public health research, or regulatory ...
Partner Research & Success Manager
Seattle, WA · On-site +1
Required Skills * 4+ years of experience working in a field which developed exposure to and understanding of real-world data (RWD), real world evidence (RWE), public health research, or regulatory ...
Required Skills * 4+ years of experience working in a field which developed exposure to and understanding of real-world data (RWD), real world evidence (RWE), public health research, or regulatory ...
Required Skills * 4+ years of experience working in a field which developed exposure to and understanding of real-world data (RWD), real world evidence (RWE), public health research, or regulatory ...
Understanding of real-world evidence (RWE) and health economics and outcomes research (HEOR) preferred. * Strong analytical and problem-solving skills. * Knowledge of clinical trial design and ...
Understanding of real-world evidence (RWE) and health economics and outcomes research (HEOR) preferred. * Strong analytical and problem-solving skills. * Knowledge of clinical trial design and ...
Director, Marketing
Seattle, WA · On-site
$150K - $175K/yr
Develop and execute a structured KOL engagement strategy that builds advocacy, informs messaging and product positioning, and generates publishable real-world evidence. * Manage advisory boards ...
Director, Marketing
Seattle, WA · On-site
$150K - $175K/yr
Develop and execute a structured KOL engagement strategy that builds advocacy, informs messaging and product positioning, and generates publishable real-world evidence. * Manage advisory boards ...
Develop and execute a structured KOL engagement strategy that builds advocacy, informs messaging and product positioning, and generates publishable real-world evidence. * Manage advisory boards ...
Develop and execute a structured KOL engagement strategy that builds advocacy, informs messaging and product positioning, and generates publishable real-world evidence. * Manage advisory boards ...
Strong understanding of real-world evidence principles, including bias, confounding, and study design considerations. * Demonstrated experience applying research methodologies, including cohort ...
Strong understanding of real-world evidence principles, including bias, confounding, and study design considerations. * Demonstrated experience applying research methodologies, including cohort ...
Strong understanding of real-world evidence principles, including bias, confounding, and study design considerations. * Demonstrated experience applying research methodologies, including cohort ...
Strong understanding of real-world evidence principles, including bias, confounding, and study design considerations. * Demonstrated experience applying research methodologies, including cohort ...
Ensures analyses meet a high standard for methodological rigor and stays current in methodology for real-world evidence studies. * Complies with data governance and data privacy policies.
Ensures analyses meet a high standard for methodological rigor and stays current in methodology for real-world evidence studies. * Complies with data governance and data privacy policies.
Data Scientist II
Seattle, WA · On-site
Ensures analyses meet a high standard for methodological rigor and stays current in methodology for real-world evidence studies. * Complies with data governance and data privacy policies.
Data Scientist II
Seattle, WA · On-site
Ensures analyses meet a high standard for methodological rigor and stays current in methodology for real-world evidence studies. * Complies with data governance and data privacy policies.
Ensures analyses meet a high standard for methodological rigor and stays current in methodology for real-world evidence studies. * Complies with data governance and data privacy policies. MINIMUM ...
Ensures analyses meet a high standard for methodological rigor and stays current in methodology for real-world evidence studies. * Complies with data governance and data privacy policies. MINIMUM ...
Research Analyst Summer Intern
Seattle, WA · Hybrid
$20/hr
This Opportunity We are seeking a Research Analyst Intern to join our team and support the generation of real-world evidence using Truveta's data platform. This role offers a unique opportunity to ...
Research Analyst Summer Intern
Seattle, WA · Hybrid
$20/hr
This Opportunity We are seeking a Research Analyst Intern to join our team and support the generation of real-world evidence using Truveta's data platform. This role offers a unique opportunity to ...
Research Analyst Summer Intern
Seattle, WA · On-site
$20/hr
This Opportunity We are seeking a Research Analyst Intern to join our team and support the generation of real-world evidence using Truveta's data platform. This role offers a unique opportunity to ...
Research Analyst Summer Intern
Seattle, WA · On-site
$20/hr
This Opportunity We are seeking a Research Analyst Intern to join our team and support the generation of real-world evidence using Truveta's data platform. This role offers a unique opportunity to ...
Lead Research Enablement Analyst
Seattle, WA · On-site +1
Build and deliver training content, webinars, workshops, and educational resources focused on EHR data, real-world evidence, and the Truveta Platform. * Work directly with customers, including ...
Lead Research Enablement Analyst
Seattle, WA · On-site +1
Build and deliver training content, webinars, workshops, and educational resources focused on EHR data, real-world evidence, and the Truveta Platform. * Work directly with customers, including ...
Build and deliver training content, webinars, workshops, and educational resources focused on EHR data, real-world evidence, and the Truveta Platform. * Work directly with customers, including ...
Build and deliver training content, webinars, workshops, and educational resources focused on EHR data, real-world evidence, and the Truveta Platform. * Work directly with customers, including ...
MSL/Sr. MSL Oncology, Multiple Myeloma (Pacific Northwest)
Seattle, WA · On-site +1
$124K/yr
Experience interpreting scientific literature, clinical trial data, or real-world evidence in a professional setting. * Experience collaborating with cross functional medical and scientific partners.
MSL/Sr. MSL Oncology, Multiple Myeloma (Pacific Northwest)
Seattle, WA · On-site +1
$124K/yr
Experience interpreting scientific literature, clinical trial data, or real-world evidence in a professional setting. * Experience collaborating with cross functional medical and scientific partners.
Real World Evidence Rwe information
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 jobs are there in clinical trials?
Jobs in clinical trials include Clinical Research Coordinators, Clinical Data Managers, Clinical Research Associates, and Study Monitors. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies, with schedules varying from standard to flexible hours.
What is RCT and RWE?
In the context of a Real World Evidence (RWE) role, RCTs (Randomized Controlled Trials) are clinical studies that randomly assign participants to different treatments to assess efficacy, while RWE involves analyzing data from real-world settings like electronic health records and insurance claims to evaluate treatment effectiveness outside controlled trials. Both are important for informing healthcare decisions and regulatory approvals, with RWE complementing RCT data by providing insights from everyday clinical practice.
What is Real World Evidence (RWE) in the healthcare industry?
Real World Evidence (RWE) refers to clinical evidence regarding the usage and potential benefits or risks of a medical product, derived from analysis of real-world data (RWD). This data is collected from sources outside of traditional clinical trials, such as electronic health records, insurance claims, patient registries, and wearable devices. RWE plays a crucial role in understanding how treatments work in routine clinical practice, informing regulatory decisions, and supporting drug development and market access. Organizations use RWE to complement clinical trial data, improving healthcare outcomes and patient care.
What are the roles in clinical trials?
In clinical trials, roles include Principal Investigator who oversees the study, Study Coordinators who manage daily operations, Data Managers who handle data collection and analysis, and Regulatory Affairs Specialists who ensure compliance with regulations. These roles require specific skills, certifications, and knowledge of Good Clinical Practice (GCP) guidelines to ensure the trial's integrity and participant safety.
What are the key skills and qualifications needed to thrive as a Real World Evidence (RWE) professional, and why are they important?
To thrive as a Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, and data analysis, often supported by an advanced degree in a relevant scientific field. Familiarity with statistical software (such as SAS, R, or Python), real-world data sources (like EHRs and claims databases), and regulatory guidelines (FDA/EMA) is essential. Strong communication, problem-solving, and cross-functional collaboration skills help convey complex findings to stakeholders and integrate RWE into decision-making. These competencies are crucial for generating credible insights that inform clinical, regulatory, and commercial strategies in the healthcare industry.
How does a Real World Evidence (RWE) professional typically collaborate with cross-functional teams in the pharmaceutical industry?
RWE professionals often work closely with colleagues from epidemiology, health economics, medical affairs, and regulatory affairs to design and execute studies using real-world data. Collaboration is essential, as RWE findings support evidence generation for regulatory submissions, market access, and post-marketing surveillance. Regular meetings, data-sharing sessions, and joint project planning are common, ensuring all stakeholders are aligned on study objectives, methodologies, and data interpretation. This collaborative environment helps translate complex data into actionable insights that support decision-making across the organization.
What is RWE in clinical research?
Real World Evidence (RWE) in clinical research refers to data collected from real-world settings outside controlled clinical trials, such as electronic health records, insurance claims, and patient registries. RWE helps researchers and healthcare professionals understand how treatments perform in routine practice and supports decision-making for drug development and regulatory approval.
What are the most commonly searched types of Real World Evidence Rwe jobs in Seattle, WA? The most popular types of Real World Evidence Rwe jobs in Seattle, WA are:
What are popular job titles related to Real World Evidence Rwe jobs in Seattle, WA? For Real World Evidence Rwe jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Real World Evidence Rwe jobs in Seattle, WA look for? The top searched job categories for Real World Evidence Rwe jobs in Seattle, WA are:
Part-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 13 days ago
Job description
Senior Director of Life Science Business Development
Truveta is the world's first health provider led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures faster, empower every clinician to be an expert, and help families make the most informed decisions about their care. Achieving Truveta' s ambitious vision requires an incredible team of talented and inspired people with a special combination of health, software and big data experience who share our company values.
Truveta was born in the Pacific Northwest, but we have employees who live across the country. Our team enjoys the flexibility of a hybrid model and working from anywhere. In person attendance is required at least once per year for an onsite meeting.
For overall team productivity, we optimize meeting hours in the pacific time zone. We avoid scheduling recurring meetings that start after 3pm PT, however, ad hoc meetings occur between 8am-6pm Pacific time. #LI-remote
Who We Need
Truveta is rapidly building a talented and diverse team to tackle complex health and technical challenges. Beyond core capabilities, we are seeking problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in the opportunity to pursue purposeful work, join a mission-driven team, and build a rewarding career while having fun, Truveta may be the perfect fit for you.
This Opportunity
Truveta is seeking a Senior Director of Life Sciences Business Development to accelerate growth within the pharmaceutical and biotechnology sectors. Reporting to the Vice President of Life Sciences Sales, this is a player/coach leadership role responsible for both individual revenue generation and leading a team of business development professionals.
The ideal candidate is a proven commercial leader who has successfully sold Real-World Data (RWD), Real-World Evidence (RWE), analytics, SaaS, or research solutions to life sciences organizations while also building, mentoring, and scaling high-performing sales teams.
This leader will carry an individual quota, directly manage a team of business development professionals, and serve as a trusted advisor to pharmaceutical, biotech, clinical development, epidemiology, HEOR, medical affairs, and data science stakeholders.
The successful candidate must be comfortable discussing complex scientific, clinical, and technical topics, including observational research, epidemiology, regulatory-grade evidence generation, AI/ML applications, healthcare data assets, and real-world data methodologies.
Responsibilities
Business Development & Revenue Leadership
Team Leadership & Coaching
Scientific & Technical Engagement
Strategic Leadership
Key Qualifications
Preferred Qualifications
Why Truveta?
Be a part of building something special. Now is the perfect time to join Truveta. We have strong, established leadership with decades of success. We are well-funded. We are building a culture that prioritizes people and their passions across personal, professional and everything in between. Join us as we build an amazing company together.
We Offer:
If you are based in California, we encourage you to read this important information for California residents linked here.
Truveta is committed to creating a diverse, inclusive, and empowering workplace. We believe that having employees, interns, and contractors with diverse backgrounds enables Truveta to better meet our mission and serve patients and health communities around the world. We recognize that opportunities in technology historically excluded and continue to disproportionately exclude Black and Indigenous people, people of color, people from working class backgrounds, people with disabilities, and LGBTQIA+ people. We strongly encourage individuals with these identities to apply even if you don't meet all of the requirements.
Please note that all applicants must be authorized to work in the United States for any employer as we are unable to sponsor work visas or permits (e.g. F-1 OPT, H1-B) at this time. We appreciate your interest in the position and encourage you to explore future opportunities with us.
Truveta is the world's first health provider led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures faster, empower every clinician to be an expert, and help families make the most informed decisions about their care. Achieving Truveta' s ambitious vision requires an incredible team of talented and inspired people with a special combination of health, software and big data experience who share our company values.
Truveta was born in the Pacific Northwest, but we have employees who live across the country. Our team enjoys the flexibility of a hybrid model and working from anywhere. In person attendance is required at least once per year for an onsite meeting.
For overall team productivity, we optimize meeting hours in the pacific time zone. We avoid scheduling recurring meetings that start after 3pm PT, however, ad hoc meetings occur between 8am-6pm Pacific time. #LI-remote
Who We Need
Truveta is rapidly building a talented and diverse team to tackle complex health and technical challenges. Beyond core capabilities, we are seeking problem solvers, passionate and collaborative teammates, and those willing to roll up their sleeves while making a difference. If you are interested in the opportunity to pursue purposeful work, join a mission-driven team, and build a rewarding career while having fun, Truveta may be the perfect fit for you.
This Opportunity
Truveta is seeking a Senior Director of Life Sciences Business Development to accelerate growth within the pharmaceutical and biotechnology sectors. Reporting to the Vice President of Life Sciences Sales, this is a player/coach leadership role responsible for both individual revenue generation and leading a team of business development professionals.
The ideal candidate is a proven commercial leader who has successfully sold Real-World Data (RWD), Real-World Evidence (RWE), analytics, SaaS, or research solutions to life sciences organizations while also building, mentoring, and scaling high-performing sales teams.
This leader will carry an individual quota, directly manage a team of business development professionals, and serve as a trusted advisor to pharmaceutical, biotech, clinical development, epidemiology, HEOR, medical affairs, and data science stakeholders.
The successful candidate must be comfortable discussing complex scientific, clinical, and technical topics, including observational research, epidemiology, regulatory-grade evidence generation, AI/ML applications, healthcare data assets, and real-world data methodologies.
Responsibilities
Business Development & Revenue Leadership
-
- Achieve and exceed individual revenue targets through direct management of strategic pharmaceutical and biotechnology accounts.
- Develop executive-level relationships with key stakeholders across clinical development, medical affairs, HEOR, epidemiology, market access, commercial analytics, and data science organizations.
- Lead complex, multi-stakeholder sales cycles from initial engagement through contract execution.
- Develop and execute territory and account strategies that drive sustainable revenue growth.
- Represent Truveta at industry conferences, scientific meetings, and customer events.
Team Leadership & Coaching
-
- Lead, coach, and develop a team of business development professionals.
- Recruit, onboard, and retain top commercial talent.
- Establish performance expectations and accountability measures that drive consistent attainment.
- Participate in strategic deal reviews, pipeline inspections, and forecasting activities.
- Foster a culture of collaboration, continuous learning, and customer-centric execution.
Scientific & Technical Engagement
-
- Engage confidently with scientific, clinical, and technical audiences regarding Truveta's data assets, research capabilities, and analytical solutions.
- Translate complex healthcare data concepts into business value for life sciences customers.
- Partner closely with Research, Product, Clinical Informatics, and Data Science teams to support customer needs and strategic opportunities.
- Maintain a deep understanding of industry trends, regulatory changes, competitive offerings, and evolving customer requirements.
Strategic Leadership
-
- Contribute to commercial strategy, market expansion initiatives, and product feedback loops.
- Provide voice-of-customer insights to executive leadership.
- Help shape go-to-market strategy and future team structure as the business scales.
- Serve as a leader and mentor across the broader Life Sciences organization.
Key Qualifications
- 10+ years of experience selling Real-World Data, Real-World Evidence, healthcare analytics, clinical research solutions, or related technology to life sciences organizations.
- 3+ years of direct people management experience with a demonstrated track record of hiring, coaching, and developing successful sales professionals.
- Proven history of exceeding revenue targets in enterprise-level life sciences sales environments.
- Strong network of relationships across pharmaceutical and biotechnology organizations.
- Demonstrated ability to engage credibly with scientific, clinical, technical, and executive stakeholders.
- Strong understanding of Real-World Data, Real-World Evidence, observational research methodologies, epidemiology, healthcare data assets, and AI-enabled analytics.
- Experience leading complex, consultative sales cycles involving multiple stakeholders and functional teams.
- Excellent communication, executive presentation, and negotiation skills.
- Willingness to travel as required.
Preferred Qualifications
- Advanced degree in a scientific, clinical, public health, healthcare, or related discipline (MS, MPH, PharmD, PhD, MD, or equivalent).
- Experience selling healthcare data, research platforms, clinical analytics, or AI-driven solutions.
- Experience building and scaling commercial teams in a high-growth environment.
- Familiarity with regulatory and evidence-generation use cases supporting pharmaceutical and biotechnology organizations.
Why Truveta?
Be a part of building something special. Now is the perfect time to join Truveta. We have strong, established leadership with decades of success. We are well-funded. We are building a culture that prioritizes people and their passions across personal, professional and everything in between. Join us as we build an amazing company together.
We Offer:
- Interesting and meaningful work for every career stage
- Great benefits package
- Comprehensive benefits with strong medical, dental and vision insurance plans
- 401K plan
- Professional development & training opportunities for continuous learning
- Work/life autonomy via flexible work hours and flexible paid time off
- Generous parental leave
- Regular team activities (virtual and in-person as soon as we are able)
- The base pay for this position is $200,000 to $240,000. The pay range reflects the minimum and maximum target. Pay is based on several factors including location and may vary depending on job-related knowledge, skills, and experience. This role is eligible for additional compensation such as incentive pay and stock options.
If you are based in California, we encourage you to read this important information for California residents linked here.
Truveta is committed to creating a diverse, inclusive, and empowering workplace. We believe that having employees, interns, and contractors with diverse backgrounds enables Truveta to better meet our mission and serve patients and health communities around the world. We recognize that opportunities in technology historically excluded and continue to disproportionately exclude Black and Indigenous people, people of color, people from working class backgrounds, people with disabilities, and LGBTQIA+ people. We strongly encourage individuals with these identities to apply even if you don't meet all of the requirements.
Please note that all applicants must be authorized to work in the United States for any employer as we are unable to sponsor work visas or permits (e.g. F-1 OPT, H1-B) at this time. We appreciate your interest in the position and encourage you to explore future opportunities with us.
About Truveta
Sourced by ZipRecruiter
Industry
Computing infrastructure providers, data processing, web hosting
Company size
51 - 200 Employees
Headquarters location
Bellevue, WA, US
Year founded
2020