Clinical Research Associate

ICON plc•Blue Bell, MA
•$91,336 - $114,170

About The Position

At ICON Strategic Solutions, the Clinical Research Associate works in a sponsor-dedicated model, supported by ICON’s global expertise. The role focuses on clinical trial monitoring for oncology/hematology studies and contributes to the development of treatments that benefit patients worldwide. The CRA is responsible for clinical trial monitoring deliverables and works collaboratively with investigators, site staff, and colleagues.

Requirements

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 1 year of experience as a Clinical Research Associate.
  • Monitoring experience with hem/onc studies.
  • 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 as required, approximately 60%.
  • Must be located in PA, NY, NJ, MA, ME, VT, NH, CT, or RI.
  • Must have the legal right to work in the country where the role is based.

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.
  • Review data 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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