... evidence strategy alignment ... You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ...
... evidence strategy alignment ... You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ...
The Quantitative Insights Lab (QuIL) within the Quantitative Medicine and Genomics organization at AbbVie is seeking a Scientific Director who will lead clinical and real world evidence (RWE ...
The Quantitative Insights Lab (QuIL) within the Quantitative Medicine and Genomics organization at AbbVie is seeking a Scientific Director who will lead clinical and real world evidence (RWE ...
The Quantitative Insights Lab (QuIL) within the Quantitative Medicine and Genomics organization at AbbVie is seeking a Scientific Director who will lead clinical and real world evidence (RWE ...
Quick apply
The Quantitative Insights Lab (QuIL) within the Quantitative Medicine and Genomics organization at AbbVie is seeking a Scientific Director who will lead clinical and real world evidence (RWE ...
Scientific Director, Clinical and Real World Evidence
North Chicago, IL · On-site
$211K/yr
The Quantitative Insights Lab (QuIL) within the Quantitative Medicine and Genomics organization at AbbVie is seeking a Scientific Director who will lead clinical and real world evidence (RWE ...
Scientific Director, Clinical and Real World Evidence
North Chicago, IL · On-site
$211K/yr
The Quantitative Insights Lab (QuIL) within the Quantitative Medicine and Genomics organization at AbbVie is seeking a Scientific Director who will lead clinical and real world evidence (RWE ...
... real-world evidence (RWE), patient-reported outcomes (PRO), and comparative effectiveness research ... The Senior Director partners cross-functionally with Medical Affairs, Clinical Development ...
... real-world evidence (RWE), patient-reported outcomes (PRO), and comparative effectiveness research ... The Senior Director partners cross-functionally with Medical Affairs, Clinical Development ...
Senior Director, Evidence Generation
Chicago, IL · On-site
$252 - $337/hr
## Senior Director, Evidence GenerationApplyremote type: Hybridlocations: Chicago, ILtime type: Full ... real-world evidence (RWE), patient-reported outcomes (PRO), and comparative effectiveness research ...
Senior Director, Evidence Generation
Chicago, IL · On-site
$252 - $337/hr
## Senior Director, Evidence GenerationApplyremote type: Hybridlocations: Chicago, ILtime type: Full ... real-world evidence (RWE), patient-reported outcomes (PRO), and comparative effectiveness research ...
Key Account Director
Chicago, IL · On-site +1
About the Role The Key Account Director will own and expand strategic partnerships with MedTech, Pharma, and industry partners engaged in Real-World Evidence (RWE) and data-driven initiatives. You'll ...
Key Account Director
Chicago, IL · On-site +1
About the Role The Key Account Director will own and expand strategic partnerships with MedTech, Pharma, and industry partners engaged in Real-World Evidence (RWE) and data-driven initiatives. You'll ...
... real-world evidence (RWE), patient-reported outcomes (PRO), and comparative effectiveness research ... The Senior Director partners cross-functionally with Medical Affairs, Clinical Development ...
... real-world evidence (RWE), patient-reported outcomes (PRO), and comparative effectiveness research ... The Senior Director partners cross-functionally with Medical Affairs, Clinical Development ...
Data Scientist
Chicago, IL · On-site
$110K - $140K/yr
This is an opportunity to work with real-world evidence (RWE), health economics and outcomes ... It's high-impact work with direct influence on healthcare decision-making, alongside recognized ...
Data Scientist
Chicago, IL · On-site
$110K - $140K/yr
This is an opportunity to work with real-world evidence (RWE), health economics and outcomes ... It's high-impact work with direct influence on healthcare decision-making, alongside recognized ...
Manager, Medical Affairs Operations
Chicago, IL · On-site +1
$130K/yr
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Manager, Medical Affairs Operations
Chicago, IL · On-site +1
$130K/yr
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Quick apply
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Global Medical Affairs Operations Manager
Mchenry, IL · On-site
$140K/yr
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Global Medical Affairs Operations Manager
Mchenry, IL · On-site
$140K/yr
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Required (All Levels) * 3+ years experience in pharmaceutical services, RWD/RWE sales, life sciences BD, healthcare technology, or evidence-generation services. * Understanding of real-world data ...
Required (All Levels) * 3+ years experience in pharmaceutical services, RWD/RWE sales, life sciences BD, healthcare technology, or evidence-generation services. * Understanding of real-world data ...
Global Medical Affairs Operations Manager
Mchenry, IL · On-site
$140K/yr
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Global Medical Affairs Operations Manager
Mchenry, IL · On-site
$140K/yr
Coordinate real-world evidence (RWE) initiatives and feasibility studies across healthcare customer ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Manager, Medical Affairs Operations
Mchenry, IL · On-site
$117 - $143/hr
Drive Real-World Evidence & Scientific Program Execution*** Coordinate real-world evidence (RWE ... Minimum 2 years of direct people leadership experience* Proven ability to manage complex cross ...
Manager, Medical Affairs Operations
Mchenry, IL · On-site
$117 - $143/hr
Drive Real-World Evidence & Scientific Program Execution*** Coordinate real-world evidence (RWE ... Minimum 2 years of direct people leadership experience* Proven ability to manage complex cross ...
Global Medical Affairs Operations Manager
Mchenry, IL · On-site
$117 - $143/hr
Drive Real-World Evidence & Scientific Program Execution * Coordinate real-world evidence (RWE ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
Global Medical Affairs Operations Manager
Mchenry, IL · On-site
$117 - $143/hr
Drive Real-World Evidence & Scientific Program Execution * Coordinate real-world evidence (RWE ... Minimum 2 years of direct people leadership experience * Proven ability to manage complex cross ...
... real-world evidence (RWE), safety/pharmacovigilance (PV) statistics, statistical programming, biomarker statistics, and advanced analytics. The role ensures consistency and scientific excellence ...
... real-world evidence (RWE), safety/pharmacovigilance (PV) statistics, statistical programming, biomarker statistics, and advanced analytics. The role ensures consistency and scientific excellence ...
Statistical Science Lead, Oncology Solid Tumor (Director Biostatistics)
Northbrook, IL · On-site
$170.45 - $243.50/hr
... real-world evidence (RWE), safety/pharmacovigilance (PV) statistics, statistical programming, biomarker statistics, and advanced analytics. The role ensures consistency and scientific excellence ...
Statistical Science Lead, Oncology Solid Tumor (Director Biostatistics)
Northbrook, IL · On-site
$170.45 - $243.50/hr
... real-world evidence (RWE), safety/pharmacovigilance (PV) statistics, statistical programming, biomarker statistics, and advanced analytics. The role ensures consistency and scientific excellence ...
Data Scientist II, Outcomes Research
Chicago, IL · On-site +1
$100K - $150K/yr
Lead and execute HEOR and real-world evidence (RWE) projects (e.g., outcomes analysis, treatment ... history may have a direct, adverse and negative relationship on the following job duties ...
Data Scientist II, Outcomes Research
Chicago, IL · On-site +1
$100K - $150K/yr
Lead and execute HEOR and real-world evidence (RWE) projects (e.g., outcomes analysis, treatment ... history may have a direct, adverse and negative relationship on the following job duties ...
Data Scientist II, Outcomes Research
Chicago, IL · On-site
$100K - $150K/yr
Lead and execute HEOR and real-world evidence (RWE) projects (e.g., outcomes analysis, treatment ... history may have a direct, adverse and negative relationship on the following job duties ...
Data Scientist II, Outcomes Research
Chicago, IL · On-site
$100K - $150K/yr
Lead and execute HEOR and real-world evidence (RWE) projects (e.g., outcomes analysis, treatment ... history may have a direct, adverse and negative relationship on the following job duties ...
Director Real World Evidence Rwe information
What is the difference between Director Real World Evidence Rwe vs Clinical Data Manager?
| Aspect | Director Real World Evidence Rwe | Clinical Data Manager |
|---|---|---|
| Credentials | Advanced degrees (PhD, MD, or Master’s), industry certifications | Bachelor’s or Master’s in life sciences, clinical research |
| Work Environment | Strategic, cross-functional teams, senior management | Data collection, database management, clinical trial sites |
| Industry Usage | Pharmaceuticals, biotech, healthcare analytics | Clinical research organizations, pharmaceutical companies |
The main difference is that the Director Real World Evidence Rwe focuses on designing and leading real-world data studies to inform healthcare decisions, while the Clinical Data Manager handles the collection and management of clinical trial data. The Rwe director has a broader strategic role, whereas the Clinical Data Manager is more operational and detail-oriented.
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For Director Real World Evidence Rwe jobs in Illinois, the most frequently searched job titles are:
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Cities in Illinois with the most Director Real World Evidence Rwe job openings:
Datavant rating
7.1
Based on 103 frontline employees who took The Breakroom Quiz
149th of 224 rated it services
Job description
Datavant is the data collaboration platform trusted for healthcare. Guided by our mission to make the world’s health data secure, accessible and actionable, we provide critical data solutions for organizations across the healthcare ecosystem - including providers, health plans, researchers, and life sciences companies. From fulfilling a single patient’s request for their medical records to powering the AI revolution in healthcare, Datavanters are building the future of how data is connected and used to improve health.
By joining Datavant today, you’re stepping onto a driven and highly collaborative team that is passionate about creating transformative change in healthcare.
Objective of the Role
The Client Partner, Real-World Evidence is responsible for driving growth with biopharma customers by leveraging Datavant’s portfolio of real-world evidence (RWE) solutions, analytics platforms, and AI platform and services. This role will partner closely with Client Partners across key accounts for co-selling, account planning, and evidence strategy alignment.
You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support regulatory, market access, and HEOR needs - representing the voice of the customer and ensuring that Datavant’s offerings meet evolving evidence generation requirements. The ideal candidate is comfortable leading complex, multi-stakeholder sales cycles and brings deep expertise in real-world data, evidence platforms, and outcomes research.
Responsibilities of the Role
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Prospect & Generate Leads: Develop and execute strategic plans to identify and target new business opportunities in biopharma, healthcare, and life sciences with a focus on organizations investing in real-world evidence strategies for regulatory submissions, market access, and clinical development.
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Build Pipeline: Proactively engage prospects via outbound calls, emails, and industry networking to build a robust pipeline of opportunities related to Aetion’s evidence generation, AI, and analytics solutions.
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Close Deals: Own the full sales process - from initial outreach to contract closure - ensuring alignment between customer evidence needs and Aetion’s RWE offerings, including the Aetion Evidence Platform (AEP) and associated data and consulting services.
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Client Engagement: Present Aetion’s value proposition in RWE and RWD analytics through compelling demonstrations and business cases that highlight regulatory-grade evidence generation, comparative effectiveness, and real-world outcomes research. Engage with senior stakeholders including heads of HEOR, RWE, Market Access, and Clinical Development.
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Collaborate Cross-Functionally: Partner with marketing, product, and science teams to deliver tailored RWE solution proposals, ensuring alignment with client data strategies, evidence frameworks, and regulatory expectations (e.g., FDA, EMA guidance).
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Market Expertise: Stay current on RWE market dynamics, technology and AI, regulatory guidance for real-world data, and competitor offerings to position Aetion as a strategic leader and partner of choice in the evidence generation ecosystem.
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Forecasting & Reporting: Maintain accurate pipeline management and forecasting in CRM systems, with attention to evidence project cycles, platform usage models, and customer expansion opportunities.
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Drive Growth: Identify new and upsell opportunities across assigned territories and existing accounts, particularly in expanding RWE adoption for post-approval studies, safety monitoring, and market access support.
Qualifications of the Role
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Proven Track Record: 6+ years of successful sales experience, ideally in healthcare, life sciences, or SaaS; with a strong preference for experience selling RWE, HEOR, or data analytics solutions. Background in selling AI is also to be considered.
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RWE Expertise: Deep understanding of real-world data sources, evidence generation methodologies, and use cases across the product lifecycle — from clinical development to commercialization.
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Hunter Mentality: Skilled at identifying, developing, and closing new RWE-focused opportunities with top biopharma clients.
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Sales Expertise: Experience managing complex, consultative sales cycles involving scientific, commercial, and data stakeholders.
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Technology/AI Skill Sets: Proven experience, knowledge, and market understanding on real AI-driven use cases for HEOR and RWE.
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Presentation Skills: Exceptional ability to communicate scientific and technical value propositions to diverse audiences, including C-suite and RWE/HEOR leadership.
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CRM Proficiency: Experienced in CRM management for tracking RWE opportunity pipelines and forecasting revenue growth.
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Industry Knowledge: In-depth knowledge of RWE market trends, regulatory guidance, and payer evidence needs is essential.
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Collaborative Team Player: Comfortable working with cross-functional science, data, and product teams in a fast-paced, mission-driven environment.
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Communication Skills: Strong written and verbal communication skills, capable of translating complex RWE concepts into impactful narratives for decision-makers.
#BC-LI1
We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.
At Datavant our total rewards strategy powers a high-growth, high-performance, health technology company that rewards our employees for transforming health care through creating industry-defining data logistics products and services.
The range posted is for a given job title, which can include multiple levels. Individual rates for the same job title may differ based on their level, responsibilities, skills, and experience for a specific job. This role is eligible for additional variable compensation.
The estimated base salary range (not including variable pay) for this role is:
$140,000—$170,000 USD
To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion.
This job is not eligible for employment sponsorship.
Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here (https://www.datavant.com/eeo-commitment-statement) . Know Your Rights (https://www.eeoc.gov/know-your-rights-workplace-discrimination-illegal) , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay.
At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren’t even able to see whether you’ve responded.) Responding is entirely optional and will not affect your application or hiring process in any way.
Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, (https://peopleteam.datavant.com/portal/en/newticket?departmentId=248697000248790029&layoutId=248697000248795462) by selecting the ‘Interview Accommodation Request’ category. You will need your requisition ID when submitting your request, you can find instructions for locating it here (https://app.tango.us/app/workflow/Greenhouse--Locating-Requisition-ID-2c7d618c8a8a423da4330ff12330695e) . Requests for reasonable accommodations will be reviewed on a case-by-case basis.
For more information about how we collect and use your data, please review our Privacy Policy (https://www.datavant.com/privacy-policy) .
About Datavant
Sourced by ZipRecruiter
Industry
Software development
Company size
51 - 200 Employees
Headquarters location
San Francisco, CA, US
Year founded
2017