About The Position

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.

Requirements

  • Bachelor's degree in a relevant field, such as life sciences or healthcare.
  • Previous experience in clinical research or a related field preferred.
  • Strong organizational and communication skills.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Attention to detail and ability to prioritize tasks effectively.
  • Must have the legal right to work in the country where the role is based.

Responsibilities

  • Support the execution and management of clinical trials.
  • Take responsibility for clinical trial monitoring deliverables, applying your skills to ensure quality and efficiency.
  • Assist in the planning, initiation, and execution of clinical trial activities.
  • Conduct site feasibility assessments and participate in site selection processes.
  • Coordinate with investigative sites to ensure compliance with study protocols and regulatory requirements.
  • Monitor study progress and data collection activities to ensure quality and accuracy.
  • Assist in the preparation and review of study documentation and reports.

Benefits

  • 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
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