Job Responsibilities Biostatistician - Real-World Evidence (RWE) Role Overview We are seeking a biostatistician with strong experience in real-world data (RWD) with observational study design and ...
Job Responsibilities Biostatistician - Real-World Evidence (RWE) Role Overview We are seeking a biostatistician with strong experience in real-world data (RWD) with observational study design and ...
The Senior Real-World Analyst (RWA) will be responsible for conducting analyses for Real-World Evidence (RWE) studies utilizing administrative claims, electronic medical records (EMR), and registry ...
The Senior Real-World Analyst (RWA) will be responsible for conducting analyses for Real-World Evidence (RWE) studies utilizing administrative claims, electronic medical records (EMR), and registry ...
Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)
New Haven, CT · On-site +1
$109K - $273K/yr
This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle. Key ...
Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)
New Haven, CT · On-site +1
$109K - $273K/yr
This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle. Key ...
Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)
New Haven, CT · On-site +1
$109K - $273K/yr
This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle. Key ...
Senior Epidemiologist, Immunology, RWE (FSP Sponsor Dedicated)
New Haven, CT · On-site +1
$109K - $273K/yr
This role will leverage secondary real-world data (RWD) sources to generate evidence that informs regulatory, safety, and clinical development decisions across the product lifecycle. Key ...
Director of Clinical Affairs - Ambulatory Monitoring and Diagnostics
Stamford, CT · On-site
$85K - $116K/yr
Architect and oversee clinical evidence programs across the product lifecycle, including early feasibility, pivotal, pre-market, post-market, registry, and real-world evidence studies. Direct study ...
Director of Clinical Affairs - Ambulatory Monitoring and Diagnostics
Stamford, CT · On-site
$85K - $116K/yr
Architect and oversee clinical evidence programs across the product lifecycle, including early feasibility, pivotal, pre-market, post-market, registry, and real-world evidence studies. Direct study ...
Support the design, execution, and interpretation of HEOR studies and real-world evidence initiatives. Assist in preparing value dossiers, payer evidence packages, and health economic models.
Support the design, execution, and interpretation of HEOR studies and real-world evidence initiatives. Assist in preparing value dossiers, payer evidence packages, and health economic models.
This role requires fluency across clinical science, real-world evidence, healthcare economics, and oncology practice operations-and the executive presence to engage C-suite, clinical leadership, and ...
This role requires fluency across clinical science, real-world evidence, healthcare economics, and oncology practice operations-and the executive presence to engage C-suite, clinical leadership, and ...
This role requires fluency across clinical science, real-world evidence, healthcare economics, and oncology practice operations-and the executive presence to engage C-suite, clinical leadership, and ...
This role requires fluency across clinical science, real-world evidence, healthcare economics, and oncology practice operations-and the executive presence to engage C-suite, clinical leadership, and ...
This role requires fluency across clinical science, real-world evidence, healthcare economics, and oncology practice operations-and the executive presence to engage C-suite, clinical leadership, and ...
This role requires fluency across clinical science, real-world evidence, healthcare economics, and oncology practice operations-and the executive presence to engage C-suite, clinical leadership, and ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
... of real-world evidence and HEOR Research & Development Demonstrates a proficient understanding of clinical study design and protocols Ensures HCPs and stakeholders receive focused and balanced ...
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.
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What are popular job titles related to Real World Evidence Rwe jobs in Connecticut? For Real World Evidence Rwe jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Real World Evidence Rwe jobs in Connecticut look for? The top searched job categories for Real World Evidence Rwe jobs in Connecticut are:
Syneos Health rating
8.1
Based on 22 frontline employees who took The Breakroom Quiz
37th of 86 rated pharmaceutical
Job description
Real World Biostatistician - RWE CMH experience
Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
Job Description
Biostatistician - Real-World Evidence (RWE)
Role Overview
We are seeking a biostatistician with strong experience in real-world data (RWD) with observational study design and safety study experience in addition to RWE CMH experience. This role will support evidence generation across multiple therapeutic areas. This role will focus on the design, analysis, and interpretation of observational studies using EMR and claims data toinform:clinical development, HEOR, regulatory strategy, and market access.
Key Responsibilities
Design and execute real-world evidence (RWE) studies using EMR and claimsdata;Conducting data specs,SAPand protocol with key research objectives
Develop and apply robust statistical methodologies, including:
Causal inference methods (e.g., propensity score methods, weighting, matching; GLM or GLMM, MMRM; survival analysis; random forest)
Trial emulation frameworks
External control arm development and borrowing strategies
Perform data analysis using healthcare coding systems (e.g., ICD, NDC)
Conduct sample size estimation and power calculations for observational and hybrid study designs
Collaborate cross-functionally with stakeholders across:
HEOR
Market Access
Regulatory
Clinical Development
Translate complex analytical results into clear, actionable insights,e.g.powerpointor study report for decision-making
Support methodological innovation in RWE, including integration of machine learning approaches where appropriate
Required Qualifications
M.S. or Ph.D. in Biostatistics, Statistics, Epidemiology, or related field
5 years of experience in RWD/RWE analytics (industry or equivalent)
Strong experience with EMR and/or claims data
Proficiencyin healthcare coding systems (e.g., ICD, NDC)
Programmingexpertisein at least one of: SAS, R, or Python
Working knowledge with SQL logic and OMOP data structures
Solid understanding of:
Causal inference methods
Observational study design
Sample size and power considerations
Some examples: Independently write cohort definitions in SQL logic; Debug data issues e.g., time zero alignment, exposure gaps; Understand concept mapping (ICD SNOMED RxNorm); Translate statisticalestimand censoring rule and data extraction logic
RWE CMH Experience
Preferred Qualifications
Ph.D. strongly preferred
Experience in one or more therapeutic areas:
Diabetes
Cardiovascular disease
Metabolic disorders
Familiarity with:
Trial emulation methodologies
External control borrowing / hybrid designs
Basic machine learning methods applied to RWD
Demonstrated ability to work across multiple therapeutic areas (TAs) in a fast-paced environment
Strong communicationand stakeholder engagement skills
Advanced (nice-to-have, not alwaysrequired)
Build reusable cohort pipelines
Optimizequeries for large-scale databases
Work across multiple CDMs (OMOP, Sentinel,PCORnet)
Core Competencies
Analytical rigor and methodological depth
Cross-functional collaboration
Ability tooperatewith agility across diverse projects and therapeutic areas
Clear and effective scientific communication
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
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About Syneos Health
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Industry
Scientific research and development services and marketing
Company size
10,000+ Employees
Headquarters location
Morrisville, NC, US