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Associate Real World Evidence Jobs in Tennessee (NOW HIRING)

With real flexibility to balance work with life moments, you're trusted to deliver results and make ... world*. As independent members of Crowe Global, Crowe LLP and Crowe Advisory LLC serve clients ...

... real-world evidence functions with reliable, compliant, and scalable technology platforms. The team operates at the intersection of IT infrastructure, clinical operations, and quality/regulatory ...

... real-world evidence functions with reliable, compliant, and scalable technology platforms. The team operates at the intersection of IT infrastructure, clinical operations, and quality/regulatory ...

... real-world evidence functions with reliable, compliant, and scalable technology platforms. The team operates at the intersection of IT infrastructure, clinical operations, and quality/regulatory ...

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Associate Real World Evidence information

What is an associate real world evidence?

An Associate Real World Evidence (RWE) professional supports the design, execution, and analysis of studies that use real-world data—such as electronic health records, insurance claims, and patient registries—to generate insights about healthcare outcomes, treatment effectiveness, and patient populations. These professionals typically work in pharmaceutical companies, research organizations, or healthcare consultancies. Their work helps guide clinical development, regulatory decisions, and health policy by providing evidence beyond traditional clinical trials. Associates often assist with data collection, statistical analysis, literature reviews, and report writing under the direction of more senior RWE scientists.

How does an associate real world evidence typically collaborate with cross-functional teams in pharmaceutical research?

As an Associate Real World Evidence (RWE) professional, you will frequently collaborate with colleagues from biostatistics, epidemiology, medical affairs, and regulatory affairs to design and execute studies using real-world data. Your role often involves translating scientific objectives into actionable study protocols, ensuring data integrity, and communicating findings to both technical and non-technical stakeholders. Effective teamwork and clear communication are crucial, as you'll contribute insights that help inform product development, regulatory submissions, and market access strategies.

What are the key skills and qualifications needed to thrive as an associate real world evidence, and why are they important?

To thrive as an Associate Real World Evidence, a strong background in epidemiology, biostatistics, or related health sciences with at least a bachelor’s or master’s degree is essential. Familiarity with statistical analysis software such as SAS or R, database management systems, and experience with healthcare or claims data are typically required. Excellent analytical thinking, attention to detail, and strong communication skills help translate complex data into actionable insights. These skills are vital for generating credible, data-driven evidence that informs healthcare decisions and supports regulatory submissions.

What is the difference between Associate Real World Evidence vs Clinical Data Analyst?

AspectAssociate Real World EvidenceClinical Data Analyst
Required CredentialsBachelor's degree in life sciences, healthcare, or related field; knowledge of RWE conceptsBachelor's degree in health informatics, statistics, or related field; proficiency in data analysis tools
Work EnvironmentPharmaceutical or healthcare companies, research organizationsHospitals, research institutions, healthcare analytics firms
Employer & Industry UsageUsed in pharmaceutical R&D, post-market studies, health outcomes researchUsed in clinical research, data management, and healthcare analytics

The Associate Real World Evidence role focuses on analyzing real-world data to support healthcare decisions, often within pharmaceutical companies. In contrast, Clinical Data Analysts primarily handle clinical trial data and statistical analysis. While both roles require strong analytical skills and related credentials, their focus areas and work environments differ, with RWE roles emphasizing observational data and post-market insights.

What are the most commonly searched types of Real World Evidence jobs in Tennessee?

The most popular types of Real World Evidence jobs in Tennessee are:

What are popular job titles related to Associate Real World Evidence jobs in Tennessee?

For Associate Real World Evidence jobs in Tennessee, the most frequently searched job titles are:

What cities in Tennessee are hiring for Associate Real World Evidence jobs?

Cities in Tennessee with the most Associate Real World Evidence job openings:

Postdoctoral Research Associate - Statistical Methods for Pediatric Oncology Clinical Trials

St. Jude Children's Research Hospital

Memphis, TN • On-site

$65 - $85/hr

Other

Posted 3 days ago

New


Key responsibilities

  • Develop innovative statistical methods for pediatric oncology clinical trials.

  • Analyze clinical trial, registry, and real-world datasets related to pediatric oncology.

  • Collaborate with pediatric oncologists, clinical investigators, statisticians, and data scientists on trial design and analysis.


St. Jude Children's Research Hospital rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

42nd of 1,065 rated hospitals


Job description

Postdoctoral Research Associate - Statistical Methods for Pediatric Oncology Clinical Trials

Location

Memphis, TN

Category

Postdoc

Department

Shift

Weekday Day

Position Type

Full Time

Scheduled Weekly Hours

40

JR7572

Job Description

We are seeking a highly motivated Postdoctoral Researcher to develop innovative statistical methods for pediatric oncology clinical trials.

The research program focuses on methodological challenges arising in pediatric and rare-disease settings, where patient populations are often small, outcomes may be delayed or complex, and conventional randomized trial approaches may not always be feasible. The successful candidate will work at the intersection of innovative clinical trial design, causal inference, external controls and real-world evidence, digital twins and counterfactual prediction, and statistical methods for survival, longitudinal, and other complex outcomes.

Clinical applications will focus primarily on pediatric solid tumors, including neuroblastoma and sarcoma, as well as emerging cellular and immunotherapy studies such as CAR-T therapy.

The position provides substantial flexibility for the postdoctoral researcher to develop an independent methodological research program based on the candidate’s background and interests, emerging scientific opportunities, and important problems arising from ongoing pediatric oncology research.

Research Areas

Potential areas of methodological research include:

Innovative Clinical Trial Design

Development of efficient and rigorous statistical methods for early- and mid-phase pediatric oncology trials, particularly in settings involving small populations, rare diseases, heterogeneous treatment response, or delayed outcomes.

Causal Inference, External Controls, and Real-World Evidence

Development of principled approaches for incorporating external information into clinical trials when concurrent randomized control groups are limited or infeasible.

Digital Twins and Counterfactual Prediction

An emerging research direction is the development and evaluation of digital twins and counterfactual prediction methods for clinical trials.

Rather than viewing a digital twin solely as a prediction model, we are interested in understanding when model-based predictions can provide clinically and statistically credible information about outcomes under alternative treatment strategies.

Survival, Longitudinal, and Complex Clinical Outcomes

Many pediatric oncology trials involve delayed, longitudinal, multistate, or otherwise complex outcomes that motivate new statistical methodology.

Your Role

The postdoctoral researcher will have opportunities to:

  • Develop new statistical methodology motivated by important pediatric oncology problems
  • Conduct simulation studies to evaluate statistical operating characteristics
  • Analyze clinical trial, registry, and real-world datasets
  • Develop statistical software in R and/or Python
  • Collaborate closely with pediatric oncologists, clinical investigators, statisticians, and data scientists
  • Participate in the design and analysis of innovative pediatric oncology clinical trials
  • Publish methodological and applied research in leading statistical, clinical trial, and medical journals
  • Present research at national and international scientific meetings
  • Develop independent research ideas and a coherent methodological research program
  • Contribute to collaborative grant proposals and future independent funding applications
  • Participate in mentoring and research activities within the Department of Biostatistics

The balance between methodological development and applied collaboration can be tailored to the candidate’s background, interests, and career goals.

Requirements

We are looking for a candidate with strong quantitative training who is interested in developing statistical methodology motivated by challenging clinical problems.

Ideal candidates will have:

  • A PhD in biostatistics, statistics, epidemiology, data science, or a closely related quantitative discipline
  • Strong training in statistical methodology
  • Experience with statistical programming, preferably in R and/or Python
  • Strong written and oral communication skills
  • Ability to work effectively in multidisciplinary research teams
  • Interest in clinical trials and biomedical research

Experience in one or more of the following areas would be particularly valuable:

  • Clinical trial design
  • Survival analysis
  • Bayesian statistics
  • Causal inference
  • External controls or real-world evidence
  • Target trial emulation
  • Longitudinal data analysis
  • Machine learning or causal prediction
  • Pediatric oncology

Prior experience in pediatric oncology is not required. Candidates with strong methodological training who are interested in developing expertise in pediatric cancer research are encouraged to apply.

St. Jude is an Equal Opportunity Employer

No Search Firms

St. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

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