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Medical Director Infectious Diseases - Europe

JR063108

About the role

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Medical Director - Infectious Diseases

Location - Poland or any EU

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. You will provide medical support to ICON project teams on clinical issues to ensure that clinical studies are conducted according to the highest ethical principles and in compliance with applicable legal and regulatory standards. This position will report to the VP Medical Affairs or designee.

Overview of the Role

  • Provide therapeutic and drug development expertise, oversee drug safety associates providing adverse event reporting, follow up on adverse events as necessary and interact with Sponsors and investigative sites on protocol medical issues.
  • Contribute to investigator meeting presentations, review study documentation, oversee safety data review and provide medical support to Business Development.
  • Senior level candidates will be expected to have prior management experience and serve as product development consultants to Clients.

Role Requirements / Skills / Experience Required

  • Medical degree
  • Board certification in Infectious Diseases
  • Minimum 2 years' experience that includes academic experience coupled with Pharmaceutical, Biotech or CRO experience.
  • Ability and willingness to travel on an as needed basis.
  • Ability to review and evaluate clinical data.
  • Excellent oral and written communication skills.

List #1

Day in the life

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

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Content type

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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.

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How Data Moves Through a Clinical Trial

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Content type

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Publish date

12/01/2025

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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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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

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

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