Associate Director, Real World Evidence (RWE) Science - Phase IV / Post-Approval (Contract) Location: United States (Remote; Eastern Time business hours preferred) Duration: 7-Month Contract ...
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Associate Director, Real World Evidence (RWE) Science - Phase IV / Post-Approval (Contract) Location: United States (Remote; Eastern Time business hours preferred) Duration: 7-Month Contract ...
Quick apply
Associate Director, Real World Evidence (RWE) Science - Phase IV / Post-Approval (Contract) Location: United States (Remote; Eastern Time business hours preferred) Duration: 7-Month Contract ...
The Clinical Data Scientist, Real World Evidence (RWE) will design and deliver advanced analytics solutions that generate robust, transparent, and scalable real-world evidence. This role operates ...
The Clinical Data Scientist, Real World Evidence (RWE) will design and deliver advanced analytics solutions that generate robust, transparent, and scalable real-world evidence. This role operates ...
The Clinical Data Scientist, Real World Evidence (RWE) will design and deliver advanced analytics solutions that generate robust, transparent, and scalable real-world evidence. This role operates ...
The Clinical Data Scientist, Real World Evidence (RWE) will design and deliver advanced analytics solutions that generate robust, transparent, and scalable real-world evidence. This role operates ...
... real-world evidence (RWE) initiatives. This role ensures alignment with global strategy while tailoring activities to US regulatory, payer, and healthcare landscapes. This role leads efforts to ...
... real-world evidence (RWE) initiatives. This role ensures alignment with global strategy while tailoring activities to US regulatory, payer, and healthcare landscapes. This role leads efforts to ...
Waltham, MA ยท On-site
Demonstrated ability to grow and nurture a real world evidence generation team * Track record of designing, conducting and publishing impactful RWE studies - primary and / or secondary * Bachelor ...
Waltham, MA ยท On-site
Demonstrated ability to grow and nurture a real world evidence generation team * Track record of designing, conducting and publishing impactful RWE studies - primary and / or secondary * Bachelor ...
Waltham, MA ยท On-site
$196K - $285K/yr
Working with the Global Medical Director, identify opportunities to generate real-world evidence (RWE) and phase IV data to address data gaps and support HCP and payer treatment decisions * Ensure ...
Waltham, MA ยท On-site
$196K - $285K/yr
Working with the Global Medical Director, identify opportunities to generate real-world evidence (RWE) and phase IV data to address data gaps and support HCP and payer treatment decisions * Ensure ...
Waltham, MA ยท On-site
$240K - $254K/yr
Real-world evidence (RWE) generation such as studies of natural history, burden of illness, treatment patterns, etc. using different data sources including claims data, electronic health records (EHR ...
Waltham, MA ยท On-site
$240K - $254K/yr
Real-world evidence (RWE) generation such as studies of natural history, burden of illness, treatment patterns, etc. using different data sources including claims data, electronic health records (EHR ...
Waltham, MA ยท On-site
OurEvidenceGenerationteamworks on high-impact, real-world HEOR projects that "move the needle" on ... Track recordof designing,conductingand publishing impactful RWE studies - primary and / or ...
Waltham, MA ยท On-site
OurEvidenceGenerationteamworks on high-impact, real-world HEOR projects that "move the needle" on ... Track recordof designing,conductingand publishing impactful RWE studies - primary and / or ...
... real-world use, including shaping risk-management strategies, integrated evidence generation ... and RWE) and perform medical review of Individual Case Safety Reports (ICSR) within the ARGUS ...
... real-world use, including shaping risk-management strategies, integrated evidence generation ... and RWE) and perform medical review of Individual Case Safety Reports (ICSR) within the ARGUS ...
... evidence generation planning, and real-world evidence approaches. The medical director will ... and RWE) and perform medical review of Individual Case Safety Reports (ICSR) within the ARGUS ...
... evidence generation planning, and real-world evidence approaches. The medical director will ... and RWE) and perform medical review of Individual Case Safety Reports (ICSR) within the ARGUS ...
... real-world use, including shaping risk-management strategies, integrated evidence generation ... and RWE) and perform medical review of Individual Case Safety Reports (ICSR) within the ARGUS ...
... real-world use, including shaping risk-management strategies, integrated evidence generation ... and RWE) and perform medical review of Individual Case Safety Reports (ICSR) within the ARGUS ...
This role is responsible for ensuring that, from clinical development through real-world evidence generation and payer engagement, we are making the strongest and best-supported arguments to secure ...
This role is responsible for ensuring that, from clinical development through real-world evidence generation and payer engagement, we are making the strongest and best-supported arguments to secure ...
This role is responsible for ensuring that, from clinical development through real-world evidence generation and payer engagement, we are making the strongest and best-supported arguments to secure ...
This role is responsible for ensuring that, from clinical development through real-world evidence generation and payer engagement, we are making the strongest and best-supported arguments to secure ...
... real-world evidence. This person will also drive evidence dissemination both internally to the Division and externally to the healthcare field. The role is globally focused with the aim of ...
... real-world evidence. This person will also drive evidence dissemination both internally to the Division and externally to the healthcare field. The role is globally focused with the aim of ...
... real-world evidence. This person will also drive evidence dissemination both internally to the Division and externally to the healthcare field. The role is globally focused with the aim of ...
... real-world evidence. This person will also drive evidence dissemination both internally to the Division and externally to the healthcare field. The role is globally focused with the aim of ...
... real-world evidence. This person will also drive evidence dissemination both internally to the Division and externally to the healthcare field. The role is globally focused with the aim of ...
... real-world evidence. This person will also drive evidence dissemination both internally to the Division and externally to the healthcare field. The role is globally focused with the aim of ...
Waltham, MA ยท On-site +1
Provides input into the design of Phase IIIB/IV studies and real-world evidence studies (RWE) to address key knowledge and evidence gaps in alignment with the integrated evidence plan (IEP)
Waltham, MA ยท On-site +1
Provides input into the design of Phase IIIB/IV studies and real-world evidence studies (RWE) to address key knowledge and evidence gaps in alignment with the integrated evidence plan (IEP)
Waltham, MA ยท On-site
$92.50K/yr
The Evidence Generation team, part of Trinity's Evidence, Value, Access and Pricing (EVAP) group ... In this role, Associateswork onhigh-impact,real-world HEOR projectsthat"movethe needle ...
Waltham, MA ยท On-site
$92.50K/yr
The Evidence Generation team, part of Trinity's Evidence, Value, Access and Pricing (EVAP) group ... In this role, Associateswork onhigh-impact,real-world HEOR projectsthat"movethe needle ...
Collaborate with HEOR, RWE, and data science teams to address unmet needs and generate impactful evidence to support access, adoption, and real-world understanding. * Support HTA, payer, and access ...
Collaborate with HEOR, RWE, and data science teams to address unmet needs and generate impactful evidence to support access, adoption, and real-world understanding. * Support HTA, payer, and access ...
Waltham, MA ยท On-site
$22/hr
Job Summary: This internship provides valuable hands-on experience and an opportunity to apply academic knowledge in a real-world setting. Location: Waltham, MA, Milwaukee, WI, or Fremont, CA ...
Waltham, MA ยท On-site
$22/hr
Job Summary: This internship provides valuable hands-on experience and an opportunity to apply academic knowledge in a real-world setting. Location: Waltham, MA, Milwaukee, WI, or Fremont, CA ...
$8.64 - $9.83
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| Aspect | Internship Real World Evidence Rwe | Data Analyst |
|---|---|---|
| Required Credentials | Typically pursuing or recent graduate in healthcare, life sciences, or related fields | Bachelor's degree in statistics, mathematics, computer science, or related fields |
| Work Environment | Healthcare or pharmaceutical companies, research organizations, or academic institutions | Various industries including finance, healthcare, marketing, and technology |
| Employer & Industry Usage | Used in pharmaceutical, biotech, and healthcare sectors for evidence generation | Widely 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.
Contractor
Posted 11 days ago
Job Title: Associate Director, Real World Evidence (RWE) Science โ Phase IV / Post-Approval (Contract)
Location: United States (Remote; Eastern Time business hours preferred)
Duration: 7-Month Contract (Full-Time, 40 hours/week)
Start: Targeting Early March 2026
We are seeking an experienced Associate Director, Real World Evidence (RWE) Science to provide coverage for a Phase IV / post-approval RWE portfolio within a global Medical Affairs environment. This is a senior-level individual contributor role requiring deep epidemiology and real-world evidence expertise, strong methodological leadership, and the ability to independently manage ongoing studies with minimal ramp-up.
This position supports global stakeholders, including Europe, and requires flexibility for early morning meetings aligned to EU collaboration.
Key Responsibilities
Lead scientific oversight of Phase IV and post-approval real-world evidence (RWE) and observational studies
Provide methodological and technical leadership for study design, feasibility assessments, and evidence planning (EU focus)
Oversee vendors/CROs conducting outsourced analyses; review protocols, statistical analysis plans, and outputs to ensure scientific rigor
Conduct and/or supervise systematic literature reviews (SLRs) and meta-analyses
Contribute to development of RWE plans aligned with regulatory, HTA, and post-approval commitments
Support retrospective analyses leveraging real-world data sources (claims, EHR, registries)
Guide protocol development for observational studies and pragmatic trials
Perform evidence reviews to inform regulatory submissions, reimbursement strategy, and medical strategy
Collaborate with Regional Medical Affairs on scientific exchange and external RWE engagement
Support development of abstracts, posters, manuscripts, and internal scientific communications
Required Qualifications
Advanced degree (MD, PhD, or MS) in Epidemiology, Biostatistics, Public Health, or related field
8โ10+ years of progressive experience in epidemiology and real-world evidence
Minimum 5 years of Pharma or Biotech industry experience
Strong expertise in:
Phase IV / post-approval epidemiologic study design
Retrospective real-world data (RWD) analyses
Observational research methodologies
Experience overseeing vendors/CROs and critically evaluating statistical methodologies
Proficiency with statistical software (R, SAS, Stata) and strong understanding of claims/EHR data structures
Demonstrated ability to work autonomously in a global, matrixed environment
Flexibility to support EU collaboration across time zones
Preferred Qualifications
Experience supporting regulatory or HTA-facing RWE deliverables
Vaccines, infectious disease, or public health epidemiology background
Experience with systematic literature reviews and meta-analyses
R programming skills, including simulations, power calculations, or Shiny applications
Experience with data extraction, cleaning, and standardization for RWD
Prior authorship of scientific publications and presentations
Experience supporting EU feasibility assessments and RWE expectations
Role Highlights
Senior-level RWE leadership without people management responsibilities
High-visibility Phase IV and real-world effectiveness portfolio
Global collaboration with strong EU engagement
Remote flexibility within the United States
Qualified candidates with deep RWE and epidemiology expertise, strong methodological grounding, and Phase IV experience in Pharma/Biotech are encouraged to apply.
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It services
201 - 500 Employees
San Mateo, CA, US
2011