Clinical Research Associate

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

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

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 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

Employment with ICON is contingent upon having the legal right to work in the country where the role is based

Minimum of 2 years of experience as a Clinical Research Associate.

Required skills

Represents the skills you have, click on the tags

Experience

2+ years