West Coast Clinical Research Associate II
On-siteArizona, United States or Oregon, United States
Job Summary
Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conduct site visits to assess performance, resolve issues, and provide support for successful trial execution. Collaborate with cross-functional teams for timely data collection and reporting, while providing training and guidance to site staff. Build effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Requires extensive experience as a Clinical Research Associate, proficiency in clinical trial software, and willingness to travel approximately 60%. This role supports ICON's mission to bring new medicines and treatments to patients faster through a values-driven approach focused on integrity and collaboration.
Required Qualifications
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate
- 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
- Site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication skills
- Interpersonal skills
- Stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
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