ICON plc

Senior Clinical Research Associate

ICON plc

full-time

Posted on:

Origin:  • 🇺🇸 United States • Arizona, California

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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
  • Ensure data integrity, participant safety, and compliance throughout the study lifecycle
  • 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

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 influence and drive compliance within a complex environment
  • Ability to travel at least 60% of the time (international and domestic - fly and drive)
  • Possess a valid driver’s license
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