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ICON

Medical Director

UK, Reading · Poland, Warsaw

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hirly's read of this role

Role family
Healthcare
Seniority
Director
Countries
GB, PL
Work mode
On-site / unstated
First seen by hirly
6 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Medical Director At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Medical Director at ICON, you will drive medical initiatives within project teams, guiding strategic direction and decision-making processes, and offer expert medical and scientific guidance, leveraging therapeutic expertise to inform project development.

What You Will Do:

You will lead medical affairs delivery across your portfolio, setting standards and developing your team.

Key responsibilities include:

  • Providing strategic medical leadership and guidance on project teams.
  • Offering expert medical and scientific consultation throughout project lifecycles.
  • Ensuring compliance with ethical, legal, and regulatory standards in medical and safety monitoring activities.
  • Representing the Medical Affairs Department in business development initiatives.
  • Providing operational oversight within the Medical Affairs Department as needed.

Your Profile:

You will bring significant medical affairs experience, with a track record of building high-performing teams and delivering results.

Required qualifications and experience:

  • Medical degree (MD) or equivalent qualification - Cardiology MD OR Endocrinology/Diabetes/Obesity or Internal Medicine MDs
  • Cardiovascular Outcomes trial experience or obesity/ GLP1 experience is a must for the role
  • Extensive experience in clinical research and development,
  • Strong understanding of clinical trial design, regulatory requirements, and GCP guidelines.
  • Exceptional analytical and problem-solving skills, with a focus on interpreting clinical data and driving evidence-based decisions.
  • Excellent leadership, communication, and collaboration skills, with the ability to work effectively in cross-functional, global teams.

#LI-remote

#LI-NR1

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .

Are you a current ICON Employee? Please click here to apply

Original posting on ICON's site ↗

Listed on hirly, a job board. hirly is not the employer: ICON is hiring for this role.

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