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Salary
≈ $30k – $77k per year (Estimated)
Location
In office (Paris)
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 30, 2026. First seen by Alion on Sep 14, 2026. ICON scores B on the Alion truth index.

Overview
Company
Impact
Profile match
ICON is an Irish clinical research organisation that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies, from early-phase trials to late-stage studies, laboratory services and real-world evidence. Founded in 1990 and listed on Nasdaq, it operates worldwide with tens of thousands of employees. The company is headquartered in Dublin, Ireland.
IHCRA

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As an IHCRA at ICON, you will support the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

What You Will Be Doing:

  • Responsible for controlling the contract full details.

  • Lead the contract negotiation, and manage site payments.

  • Good experience with VeeVa Systems

  • Knowledge of Ariba, Apex, RGPS and Grant Plan

  • Coordinating the day-to-day operations of clinical studies, including site management, participant recruitment, and data collection.

  • Ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines throughout the study lifecycle.

  • Providing training and support to site staff and investigators on study protocols and operational procedures.

Your Profile:

  • Advanced degree in a relevant field such as life sciences, nursing, or healthcare administration.

  • Extensive experience in clinical study coordination or clinical trial management, preferably within the pharmaceutical or biotechnology industry.

  • Strong understanding of clinical trial processes, regulatory requirements, and GCP.

  • Excellent organizational skills and attention to detail, with the ability to manage multiple studies simultaneously.

  • Strong communication and interpersonal skills, with the ability to work collaboratively with diverse teams and stakeholders.

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

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