Clinical Research Coordinator

ICON plc•Cambridge, MA
•$56,704 - $70,880

About The Position

At ICON Strategic Solutions, the Clinical Research Coordinator works in a sponsor-dedicated model and is supported by ICON’s global expertise. The role supports the execution and management of clinical trials and contributes to the development of treatments and therapies. It takes responsibility for clinical trial monitoring deliverables, helping ensure quality and efficiency.

Requirements

  • Bachelor's degree in a relevant field, such as life sciences or healthcare.
  • 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.
  • Employment requires the legal right to work in the country where the role is based.

Nice To Haves

  • Previous experience in clinical research or a related field is preferred.
  • Relevant clinical trial monitoring experience.

Responsibilities

  • Assist in planning, initiating, and executing 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 preparing and reviewing study documentation and 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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