Clinical Research Associate

ICON plc•Washington, NV
•$91,336 - $114,170

About The Position

As a Clinical Research Associate II at ICON Strategic Solutions, you will work in a sponsor-dedicated model supported by ICON’s global expertise. You will contribute to clinical trial monitoring activities, take responsibility for your deliverables, and collaborate with others. The client is seeking candidates with experience monitoring ophthalmology trials or multiple therapeutic areas. The role requires approximately 60% travel.

Requirements

  • Bachelor's degree in a scientific or healthcare-related field.
  • At least 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Willingness to travel approximately 60%.
  • Legal right to work in the country where the role is based.

Nice To Haves

  • Experience monitoring ophthalmology trials or trials across multiple therapeutic areas.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborate with investigators and site staff to facilitate smooth study conduct.
  • Perform data review and resolve queries to maintain high-quality clinical data.
  • Contribute to the preparation and review of study documentation, including protocols and clinical study reports.

Benefits

  • Competitive base salary and performance-related incentives.
  • 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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