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 ...
Raritan, New Jersey, United States of America We are searching for the best talent for Director, Global Real World Evidence (RWE). About Innovative Medicine Our expertise in Innovative Medicine is ...
Raritan, New Jersey, United States of America We are searching for the best talent for Director, Global Real World Evidence (RWE). About Innovative Medicine Our expertise in Innovative Medicine is ...
The Director of Global Real-world Evidence (RWE) is a stretegic leadership role within the Global Medical Affairs organization, supporting enterprise and therapeutic area priorities through the ...
The Director of Global Real-world Evidence (RWE) is a stretegic leadership role within the Global Medical Affairs organization, supporting enterprise and therapeutic area priorities through the ...
Raritan, New Jersey, United States of America We are searching for the best talent for Director, Global Real World Evidence (RWE). About Innovative Medicine Our expertise in Innovative Medicine is ...
Raritan, New Jersey, United States of America We are searching for the best talent for Director, Global Real World Evidence (RWE). About Innovative Medicine Our expertise in Innovative Medicine is ...
You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ... evidence generation requirements. The ideal candidate is comfortable leading complex, multi ...
You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ... evidence generation requirements. The ideal candidate is comfortable leading complex, multi ...
You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ... evidence generation requirements. The ideal candidate is comfortable leading complex, multi ...
You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ... evidence generation requirements. The ideal candidate is comfortable leading complex, multi ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... 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 ...
... evidence strategy alignment ... You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ...
Quick apply
... 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 ...
... evidence strategy alignment ... You will serve as a trusted advisor on the use of real-world data (RWD) and RWE to support ...
Real World Evidence Rwe information
What is real world evidence (RWE)?
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.
How does a real world evidence (RWE) professional collaborate with cross-functional teams?
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 are the key skills and qualifications needed to thrive as a real world evidence (RWE) professional?
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.
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.
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Job description
Job Title: 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 (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
8–10+ 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.
About Ubertal
Sourced by ZipRecruiter
Industry
It services
Company size
201 - 500 Employees
Headquarters location
San Mateo, CA, US
Year founded
2011