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Remote Real World Evidence Rwe Jobs in Kentucky (NOW HIRING)

US or Canada (Hybrid/Remote) Position Overview The Research Associate/Senior Research Associate, Real World Evidence (RWE) is part of the global Real World & Late Phase (RWLP) Business Unit ...

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Remote Real World Evidence Rwe information

What are Remote Real World Evidence (RWE) jobs?

Remote Real World Evidence (RWE) jobs involve gathering, analyzing, and interpreting data from real-world sources—such as electronic health records, insurance claims, patient registries, and wearable devices—to inform healthcare decisions. Professionals in these roles typically work for pharmaceutical companies, research organizations, or healthcare technology firms. Remote RWE jobs allow employees to contribute to research and data analysis from home or other off-site locations, using digital tools to collaborate with teams and stakeholders. These positions are crucial for understanding how medical treatments perform outside of controlled clinical trials, ultimately improving patient care and supporting regulatory submissions.

What is the difference between Remote Real World Evidence Rwe vs Remote Data Analyst?

AspectRemote Real World Evidence RweRemote Data Analyst
Required CredentialsAdvanced degrees in healthcare, epidemiology, or biostatistics; experience with RWE methodologiesBachelor's or master's in data science, statistics, or related fields; proficiency in data analysis tools
Work EnvironmentCollaborates with healthcare providers, pharma companies, and regulatory agencies; focuses on healthcare dataWorks across industries; analyzes large datasets to inform business decisions
Industry UsagePrimarily in healthcare, pharmaceuticals, and regulatory sectorsAcross various sectors including finance, marketing, and healthcare

Remote Real World Evidence Rwe specialists focus on analyzing healthcare data to generate evidence for medical and regulatory decisions, requiring healthcare-specific knowledge. Remote Data Analysts handle diverse datasets across industries, emphasizing data processing and reporting skills. While both roles involve data analysis, RWE roles are more specialized in healthcare and regulatory contexts.

What is a RWE scientist?

A RWE (Real World Evidence) scientist is a professional who analyzes real-world data from sources like electronic health records, claims databases, and patient registries to generate evidence on the effectiveness, safety, and value of healthcare interventions. They typically have expertise in biostatistics, epidemiology, and data analysis tools such as SAS or R, and work within healthcare, pharmaceutical, or research organizations to support decision-making and regulatory submissions.

What is RWE real world evidence?

Real World Evidence (RWE) in the context of a Remote Real World Evidence (RWE) role refers to the clinical evidence derived from analyzing data collected outside traditional clinical trials, such as electronic health records, claims data, and patient registries. Professionals in this field interpret this data to support healthcare decision-making, regulatory submissions, and product development, often using data analysis tools and statistical methods.

What is the most entry level job in clinical research?

The most entry-level job in clinical research is often a Clinical Research Assistant or Coordinator, responsible for supporting study activities, data collection, and documentation. These roles typically require basic knowledge of clinical trial processes, strong organizational skills, and may involve training on specific research tools or protocols.

What are the key skills and qualifications needed to thrive as a Remote Real World Evidence (RWE) professional, and why are they important?

To thrive as a Remote Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, or related life sciences, typically supported by an advanced degree (e.g., MPH, MS, PhD). Familiarity with statistical software such as SAS, R, or Python, and experience working with large healthcare databases and electronic health records are crucial. Excellent analytical thinking, problem-solving abilities, and effective communication skills help translate complex data into actionable insights for stakeholders. These competencies ensure the generation of robust, real-world data analyses that inform healthcare decisions and regulatory submissions.

What is the highest paying job in clinical research?

In clinical research, senior roles such as Clinical Research Director or Vice President of Clinical Operations tend to be the highest paying, often earning six-figure salaries. These positions require extensive experience, leadership skills, and knowledge of regulatory requirements and industry standards.

What are some common challenges faced by Remote Real World Evidence (RWE) professionals and how can they be addressed?

Remote RWE professionals often encounter challenges such as managing large and diverse datasets, ensuring data privacy, and coordinating effectively with cross-functional teams across different time zones. To address these, it's important to have strong data management skills, familiarity with relevant regulations (like GDPR or HIPAA), and effective communication tools. Actively engaging in regular virtual meetings and leveraging collaborative platforms can help maintain alignment with stakeholders and ensure project milestones are met.
What are the most commonly searched types of Real World Evidence Rwe jobs in Kentucky? The most popular types of Real World Evidence Rwe jobs in Kentucky are:
What are popular job titles related to Remote Real World Evidence Rwe jobs in Kentucky? For Remote Real World Evidence Rwe jobs in Kentucky, the most frequently searched job titles are:
What job categories do people searching Remote Real World Evidence Rwe jobs in Kentucky look for? The top searched job categories for Remote Real World Evidence Rwe jobs in Kentucky are:
What cities in Kentucky are hiring for Remote Real World Evidence Rwe jobs? Cities in Kentucky with the most Remote Real World Evidence Rwe job openings:
Senior Research Associate

Senior Research Associate

Syneoshealth

Canada, KY • On-site, Remote

Full-time

Posted 8 days ago


Syneos Health rating

8.3

Company rating: 8.3 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

24th of 73 rated pharmaceutical


Job description

Senior Research Associate

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 TITLE: Research Associate/Senior Research Associate, Real World Evidence

SELECT ONE: Clinical Solutions

JOB CODE: SH1317/ SH1323

REPORTS TO: Associate Director, Real World Evidence; or designee

Business Unit: Real World & Late Phase (RWLP)
Industry: Life Sciences
Location: US or Canada (Hybrid/Remote)

Position Overview

The Research Associate/Senior Research Associate, Real World Evidence (RWE) is part of the global Real World & Late Phase (RWLP) Business Unit, supporting the generation of real-world evidence, and patient outcomes evidence across the drug development lifecycle.

In this role, you will contribute to and or lead real-world research initiatives that inform clinical strategy, regulatory engagement, and market access decisions for life sciences clients. Working closely with senior team members, you will support the design and execution of retrospective and prospective studies while developing your expertise in RWE and outcomes research methodologies.

This position is well suited to professionals seeking meaningful exposure to or to deepen their expertise in evidence generation within a collaborative, well-supported team environment that values high-quality work and sustainable performance.

Key Responsibilities

  • Contribute to study design and methodology development
  • Develop innovative approaches, frameworks and solutions to client problems
  • Deliver project outputs that meet established quality standards, timelines, and budget requirements.
  • Conduct structured literature reviews and targeted secondary research to support RWE initiatives.
  • Participate in qualitative research activities, including patient interviews, to generate actionable healthcare insights.
  • Analyze and interpret qualitative and quantitative 'real-world' data for deliverables
  • Conduct workshops and moderate discussions
  • Present results to external clients
  • Contribute to the development of:
    • Study protocols
    • Technical reports
    • Manuscripts and scientific posters
    • Client presentations
  • Develop and format materials using PowerPoint, Word, and Excel.
  • Summarize and synthesize complex clinical and outcomes data into clear, structured findings.
  • Support retrospective and prospective real-world studies under senior guidance.
  • Demonstrate openness to leveraging emerging technologies, including AI-enabled tools, to improve efficiency, analytical rigor, and personal productivity.

Qualifications

Required

  • Master's degree in public health, epidemiology, health sciences, or a related field (or equivalent combination of education and experience).
  • 1-2 years (Research Associate), or 2+ years (Senior Research Associate) of relevant experience within the life sciences industry (e.g., HEOR, RWE, clinical research, pharmaceutical industry, healthcare consulting, or academia).
  • Foundational understanding of real-world research methodologies and study design.
  • Overall understanding of the drug development lifecycle.
  • Strong analytical and critical thinking skills.
  • Proficiency in Microsoft Excel, Word, and PowerPoint.
  • Working knowledge of statistical software (e.g., SAS, R, Stata, or similar).
  • Business-level conversational English (written and spoken).

Preferred

  • Graduate degree (Master's or PhD) in a relevant discipline.
  • Academic or industry research experience.
  • Conducting analyses in databases and/or registries

Key Competencies

  • Clear and professional communication skills
  • Strong teamwork and collaboration
  • Attention to detail and commitment to quality
  • Ability to manage multiple priorities in a structured, deadline-driven environment
  • Intellectual curiosity and commitment to continuous improvement, including adoption of new technologies
  • Willingness to travel (~10%)

Work Environment

As part of a global RWLP team, you will work within an international, cross-functional environment with access to experienced mentors and structured development opportunities. Our hybrid model offers flexibility, and our team culture emphasizes high standards, collaboration, and sustainable performance to support long-term career growth in the life sciences industry.

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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