ICON plc

Senior Clinical Research Associate – CST

ICON plc

full-time

Posted on:

Origin:  • 🇺🇸 United States • Illinois

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Job Level

Senior

Tech Stack

Google Cloud Platform

About the role

  • Oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
  • Ensure data integrity, participant safety, and compliance throughout the study lifecycle.

Requirements

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • Extensive experience as a Clinical Research Associate with strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously.
  • Strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management.
  • Proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive).
  • Valid driver’s license.
  • Knowledge of Good Clinical Practice (GCP) standards.
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