West Coast Clinical Research Associate II

Responsibilities

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

Benefits

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
• Glassdoor
• 3.7
• Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
• Dublin, Dublin, IRL
• https://www.iconplc.com
• Public Company
• Total Funding
• $4.15B
• 2026-08-06
• Post Ipo Debt· $2.15B
• 2024-04-30
• Post Ipo Debt· $2B
• 1998-05-15
• IPO
• Leadership Team
• Barry Balfe
• Chief Executive Officer
• Martin Lachs
• Senior Vice President, Oncology Program Management
• Recent News
• SiliconANGLE
• AI safety worries multiply but everyone’s still racing full speed ahead
• 2026-10-17
• FierceBiotech

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
• Willingness to travel as required (approximately 60%)

Required skills

• Clinical Practice (GCP), Clinical Trial Monitoring, Clinical Trial Processes, Clinical Trial Software, Data Integrity, Regulatory Requirements, Site Management, Stakeholder Management

Experience

• Mid level