Clinical Research Associate II

Responsibilities

• You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively
• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
• Collaborating with investigators and site staff to facilitate smooth study conduct
• Performing data review and resolution of queries to maintain high-quality clinical data
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Benefits

• Remote - United States
• 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
• Distribution of Different Job Fields Receiving Sponsorship
• Represents job field similar to this job
• Engineering and Development
• Product Management
• Legal and Compliance
• Management and Executive
• Trends of Total Sponsorships
• *2026
• (7)
• 2025
• (4)
• 2024
• 2023
• (5)
• 2022
• (11)
• 2021

Qualifications

• Bachelor's degree in a scientific or healthcare-related field
• Minimum of 2 years of experience as a Clinical Research Associate
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
• Strong organizational and communication skills, with attention to detail
• Ability to work independently and collaboratively in a fast-paced environment
• Minimum of 2 years of experience as a Clinical Research Associate.

Required skills

• Clinical Trial Monitoring, Clinical Trial Processes, Clinical Trial Regulations, ICH-GCP

Experience

• 2+ years