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Associate Epidemiologist - RWE

JR067771

About the role

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Associate Epidemiologist

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

We are looking for passionate, resilient, and inspiring individuals to join our team. As an Associate Epidemiologist, you will provide methodological expertise relating to the design and conduct of studies, will perform or support the analyses, and will contribute to reporting and interpreting the findings.

The role

  • Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
  • As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.
  • Travel (approximately 15%) domestic and/or international
  • Take responsibility for co-ordinating own workload and embrace teamwork approach in an LPOR department
  • Contribute to marketing activities as appropriate
  • Establish and maintain client relationships
  • Contribute to building business links within LPOR and with ICON Clinical Research
  • Assist in proposal writing, project work and client liaison
  • Contribute to publications/scientific communications as appropriate
  • Demonstrate and actively promote an open and honest working environment to encourage close teamwork and foster knowledge transfer
  • Responsible for ensuring compliance with all relevant SOPs, policies and procedures
  • Such other duties and tasks as are allocated to you at the reasonable discretion of the Company

What you need

  • A bachelor's degree or equivalent as relevant, Master's degree preferred Epidemiology Or BioStats preferred
  • A demonstrable experience in literature reviews and evidence synthesis
  • Experience / familiarity with one or more of the following statistical packages (R, STATA, SAS, WinBUGs)
  • Excellent oral and written communication skills.
  • Accuracy, attention to detail and time management skills.

List #1

Day in the life

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Leading Through Change: Zhong Yao's Journey at ICON in China

Teaser label

Our People

Content type

Blogs

Publish date

12/10/2025

Summary

Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.

Teaser label

From culture to collaboration, Zhong Yao explains how ICON China delivers quality clinical trials, and empowers local talent.

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How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

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Publish date

12/01/2025

Summary

How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i

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Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

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Quality and Compliance - A Plain Language Guide

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Industry

Content type

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Publish date

11/28/2025

Summary

Quality and Compliance for New Entrants:           A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job

Teaser label

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

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