Clinical Research Associate II

ICON plc is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster. The Clinical Research Associate II supports clinical trials by conducting site visits, ensuring protocol compliance and patient safety, collaborating with investigators, reviewing clinical data, and contributing to study documentation.

Responsibilities

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

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.

Company

Clinical research organization providing outsourced drug and device development services

Dublin, Dublin, IRL

https://www.iconplc.com/

Founded in 1990

10001+ employees

Qualifications

Bachelor's degree in a scientific or healthcare-related field

Minimum of 1-year independent monitoring to be considered for a Clinical Research Associate II

a minimum of 3 years independent monitoring to be considered for a Senior 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

A minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate

a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

Required skills

Clinical Trial Processes, Clinical Trial Monitoring, ICH-GCP Guidelines, Clinical Trial Regulations, Clinical Data Review

Experience

1+ years