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Associate Real World Evidence Jobs in Kentucky (NOW HIRING)

$150 - $190/hr

Work closely with data and analytics teams to incorporate real-world evidence and insights that enhance patient engagement and retention. * Ensure compliance with industry standards, data security ...

$140 - $190/hr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for ...

$190 - $250/hr

A collaborative, "learn-it-all" partner who seeks feedback, iterates on methods, and stays current on statistical best practices in clinical, digital health, and real-world evidence settings. * An ...

New

$196 - $261/hr

... evidence across multiple sources, including real-world data, literature, expert input, field-based insights, and emerging analytics tools. * Identify novel approaches to insight mining, including ...

Posted today

$55 - $75/hr

## Clinical Account Associate, DallasApplylocations: Remote - Texastime type: Full timeposted on ... Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ...

New

$109 - $273/hr

We bring together scientific expertise and real-world data to help sponsors make decisions and accelerate evidence generation to improve patient outcomes. In this role, you'll work closely with one ...

$112 - $168/hr

## Associate Director, Global Category SourcingBoston, Massachusetts, United States of AmericaApply ... Real-World Evidence generation studies and understanding of epidemiological study designs • ...

$65 - $90/hr

## Clinical Account Associate, Blue RidgeApplylocations: Remote - North Carolina: Remote ... Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ...

New

$148 - $201/hr

Do you like to work within scientific and commercial teams to generate real-world evidence (RWE ... Associate's degree and 10 years of data sciences and scientific experience OR* High school diploma ...

New

$66 - $94/hr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real ... We are seeking a Portfolio Strategy Associate to join our team. This role provides targeted ...

New

$120 - $170/hr

Associates are part of a stimulating and exciting environment in which they can develop their ... real world evidence into real life practice to meet customer needs. * Gather and report medical ...

$69 - $101/hr

... real-world evidence (RWE), and digital clinical trials * Experience with data platform design ... Associate Level 82,025.00 - 101,325.00 for the Consultant Level #J-18808-Ljbffr

$210 - $230/hr

Deworm the World has delivered over 2 billion treatments, significantly reducing worm prevalence ... steward of evidence in real implementation settings, not primarily as an academic researcher.

$183 - $248/hr

Lead or support global evidence-generation activities, including real-world evidence and other ... Associate's degree and 10 years of Medical Affairs experience * High school diploma / GED and 12 ...

$55 - $70/hr

Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for ...

New

$114 - $170/hr

Stay current with trends in real-world evidence, digital health data, AI, GenAI, agentic AI, data mesh, and evolving regulatory expectations, and contribute to pilots that improve how medical affairs ...

$163 - $216/hr

Maintain deep knowledge of Veradigm Real World Evidence solutions and data offerings and the ... Veradigm believes in empowering our associates with the tools and flexibility to bring the best ...

New

$80 - $110/hr

... real world evidence data and analytics. Partnering with providers, health plans, and life sciences companies, including CMS' GUIDE dementia care model, Synapticure is dedicated to transforming the ...

New

$175 - $195/hr

... real world evidence into clear, credible, and compliant education and messaging. This role will establish, build, and scale the Medical Affairs and Medical Education capability within the ...

$177 - $294/hr

Appropriately prioritizes the needs of the customer and of Pfizer Oncology to develop and implement objective and scientifically sound Real World Evidence-based outcomes tools (such as Health ...

Showing results 41-60

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 Kentucky?

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

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

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

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

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

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

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

Sr. Director, Product Management - Patient Access Technology

UBC

On-site

$150 - $190/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago


United Brotherhood Of Carpenters rating

8.6

Company rating: 8.6 out of 10

Based on 29 frontline employees who took The Breakroom Quiz

2nd of 12 rated unions


Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Regular Information Technolo All Virtual Locations, Home Based Position, USA, Remote, US

Today Requisition ID: 7580

NOTE: This position REQUIRES familiarity with Specialty Pharmacy Services, Patient Access Programs, or Affordability Solutions (e.g., copay cards, patient assistance programs).

As a leader in the pharmaceutical support industry, UBC is committed to empowering health solutions for a better tomorrow . We take pride in improving patient outcomes and advancing healthcare. At UBC, we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation.

Embark on a rewarding career journey with UBC! Grow your career while making a meaningful impact on the world around you. UBC fosters a culture built on our Core Values of Respect, Accountability, Innovation, Quality, Integrity, and Collaboration. We believe in an inclusive workplace that fosters creativity.

If you are seeking a career that will challenge, inspire, and reward you, join us at UBC!

Brief Description :

We are seeking a Senior Director of Product Management to lead the definition of technology solutions that support UBC’s Patient Services offerings, specifically focusing on Patient Access, Adherence, and Affordability. In this role, you will define the why and what of new products and act as the strategic bridge between business stakeholders, operations and technology leadership, industry leaders, and clients, ensuring our products deliver measurable value to patients, clients, and care providers. You will lead the definition of the product vision, prioritization of the product backlog, and translating business needs into actionable requirements for the development teams. You will represent and/or oversee communications related to critical and strategic clients and work with internal teams and external clients to continue ongoing business, enhance and improve our product offerings, and grow UBC’s book of business.

Specific job duties:

  • Continuously monitor industry trends, competitive landscape, and emerging technologies to inform product strategy and maintain market relevance.
  • Inform and communicate the product vision, roadmap, and value proposition for UBC solutions supporting patient access, adherence, and affordability.
  • Own and manage the product backlog to ensure development efforts are aligned with strategic business goals, client needs, and patient-centric outcomes.
  • Collaborate with internal stakeholders (e.g., operations, project management, regulatory, development, quality) to gather, refine, and prioritize requirements.
  • Act as the primary liaison between business stakeholders and agile development teams, ensuring clear user stories, acceptance criteria, and feedback loops.
  • Engage regularly with clients and key stakeholders to deeply understand their needs, pain points, and priorities, ensuring the product backlog reflects real-world user requirements.
  • Collaborate with finance and pricing teams to understand product cost structures, pricing strategies, and profitability drivers, ensuring business viability informs product decisions.
  • Partner with marketing to develop and refine go-to-market strategies, ensuring product positioning, messaging, and launch plans are aligned with customer needs and business objectives.
  • Ensure project, scrum, and business teams are aware of new product enhancements and functionality.
  • Work closely with data and analytics teams to incorporate real-world evidence and insights that enhance patient engagement and retention.
  • Ensure compliance with industry standards, data security, and healthcare regulations, including HIPAA.
  • Contribute to business development activities including RFI and RFP responses, project pricing and estimation, client presentations, and strategic planning.
  • Monitor product performance, user feedback, industry trends, and competitor activityto drive continuous improvement and keep the product portfolio aligned with current market expectations.
  • Collaborate with project management and delivery leadership during program startup to ensure approved scope, product intent, client commitments, decision history, budget assumptions, risks, dependencies, and stakeholder expectations are clearly transferred to the delivery organization.
  • Serve as an executive-facing productsolution leader in strategic client meetings, bid defenses, governance forums, quarterly business reviews, and portfolio-level client discussions where future functionality, scope, roadmap direction, or product investment may be discussed.
  • Ensure proposed client commitments are evaluated for scope, feasibility, regulatory impact, validation impact, budget requirements, resource needs, and delivery risk before commitments are finalized.
  • Sponsor business cases and technology/AI governance review materials that define product objectives, target users/stakeholders, expected value, costs, dependencies, risks, assumptions, success measures, and decision points.
  • Partner with architecture, engineering, information security, privacy, quality, compliance, and data governance stakeholders to ensure product direction aligns with enterprise standards and regulated-life-sciences operating requirements.
  • Establish relationships with Pharma clients to develop co-definition, co-development, idea exchange, and early adoption outside of traditional engagement during the RFP process.

Supervisory Responsibility:

May manage Product Business Analysts.

Desired Skills and Qualifications:

  • Bachelor’s degree in Life Sciences, Computer Science, Business, Healthcare Administration, or related field (Master’s preferred).
  • 8+ years of experience as a Product Manager, preferably in healthcare, life sciences, or patient support services. Certification as a Product Owner (CSPO) or equivalent is a plus.
  • Familiarity with specialty pharmacy services, patient access programs, or affordability solutions (e.g., copay cards, patient assistance programs).
  • Ability to make difficult product decisions and prioritize features based on business value
  • Experience with backlog management and user story writing.
  • Excellent skills in translating complex business needs into clear product requirements and user stories.
  • Strong communication, collaboration, and stakeholder management abilities.
  • Ability to balance technical constraints, business priorities, and regulatory requirements.
  • Passionate about delivering high-quality software products
  • Customer-focused mindset
  • Collaborative team player
  • Resilient under pressure and adaptable to changing priorities and requirements
  • Excellent time management and organizational skills

At UBC, employee growth and well-being are always at the forefront. We offer an extensive range of benefits to ensure that you have everything you need to thrive personally and professionally. Here are some of the exciting perks UBC offers:

  • Remote opportunities
  • Growth opportunities for promotion
  • 401K with company match
  • Tuition reimbursement (after 90 days of employment)
  • Flexible work environment
  • Discretionary PTO (Paid Time Off)
  • Paid Holidays
  • Employee assistance programs
  • Medical, Dental, and vision coverage
  • HSA/FSA
  • Wellness program
  • Adoption assistance
  • Short-term disability (after 90 days of employment)
  • Long-term disability
  • Life insurance

UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, or basis of disability or any other federal, state, or local protected class. We are committed to a diverse, equitable, and inclusive culture that fosters respect for each other, our clients, and our patients.

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