West Coast Clinical Research Associate II

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a CRA II at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Pharmaceuticals

• Insider Connection @ICON Strategic Solutions
• 2 email credits available today
• Beyond your network
• Nicole B. & 4 connections
• From your previous company
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• from your School
• Sadhana Narava
• Lead Site Activation Manager (LSAM)
• @Sri Venkateswara University
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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

• Competitive and performance related incentives
• Health and wellbeing programmes including 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
• Benefits may vary depending on role and location
• ICON Strategic Solutions is the global leading provider of Functional Service Provision (FSP) services.
• Dublin , GB
• https://www.iconplc.com/services/strategic-solutions/
• Late Stage
• Leadership Team
• Jennifer Alamo Linnell
• VP, Human Resources Business Partner
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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