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Associate Real World Evidence Jobs in Tennessee (NOW HIRING)

R1

PRN/AS NEEDED -Patient Access Assoc I

Waverly, TN · On-site

$16 - $21.10/hr

At R1,you'llbe part of a mission-driven team that blends advanced technology with real-world ... Our associates are given the chance to contribute, think boldly and create meaningful work that ...

R1

PRN/AS NEEDED -Patient Access Assoc I

Waverly, TN · On-site

$16 - $21.10/hr

At R1, you'll be part of a mission-driven team that blends advanced technology with real-world ... Our associates are given the chance to contribute, think boldly and create meaningful work that ...

Frasco Inc

Surveillance Investigator

Memphis, TN · On-site

$20 - $26/hr

Get paid to learn the ropes of fraud investigation and real-world surveillance. Frasco offers fully ... Prepare detailed reports with timestamps and supporting evidence for legal use * Adapt to changing ...

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Associate Real World Evidence information

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 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 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.

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 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 job categories do people searching Associate Real World Evidence jobs in Tennessee look for?

The top searched job categories for Associate Real World Evidence jobs in Tennessee 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:

Associate Real World Evidence jobs near you

Professor (Legal & Healthcare) - AI Trainer

micro1 AI

Memphis, TN • Remote

$20 - $55/hr

Part-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Job Title: Academic Researcher


Job Type: Contractor


Location: Remote


Job Summary: In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input.


Key Responsibilities:

  1. Conduct in-depth research and analysis in your area of expertise, delivering high-quality, evidence-based insights.
  2. Prepare, format, and review complex documents in Word and PDF, utilizing advanced features such as tracked changes, form filling, and data extraction.
  3. Collaborate with cross-functional teams, including legal, healthcare, policy, and finance professionals, to support diverse project needs.
  4. Translate complex research findings into clear, concise reports and presentations tailored for Fortune 500 standards.
  5. Evaluate and synthesize academic literature, legal documents, or industry data to inform project outcomes.
  6. Ensure accuracy, consistency, and compliance with designated guidelines in all written deliverables.
  7. Maintain clear and professional written and verbal communication with project stakeholders and team members.


Required Skills and Qualifications:

  1. Minimum 3+ years of relevant professional experience in academic research, legal, policy, healthcare, or related sectors.
  2. Master’s degree, PhD, or JD from a recognized institution.
  3. Demonstrated expertise in preparing and reviewing Word and PDF documents (tracked changes, formatting, data extraction, document review).
  4. Outstanding written and verbal communication skills; meticulous attention to detail.
  5. Ability to manage multiple priorities in a remote, deadline-driven environment.
  6. Experience collaborating with multidisciplinary teams on complex deliverables.
  7. Proven record of producing high-quality, client-ready outputs.


Preferred Qualifications:

  1. Experience working with or for Fortune 500 companies.
  2. Prior involvement in legal, healthcare, policy, or financial operations document workflows.
  3. Active publication or presentation record in academic or industry settings.

Apply