Full-time
Clinical Research Associate
Competitive
Entry, Mid, Senior LevelScience & PharmaceuticalPosted 30+ Days Ago
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Role overview
Job type
Salary
Competitive
Location
Sector
Posted
30+ Days Ago
Job description
ICON Strategic Solutions is a sponsor-dedicated clinical research organization that provides global expertise and supports the development of treatments benefiting patients worldwide. The Clinical Research Associate will conduct and monitor clinical trials in multiple therapeutic areas, including oncology, while ensuring protocol compliance, data integrity, and patient safety. The role also involves collaborating with clinical sites, reviewing data, and preparing 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
Competitive base salary 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
Company
Outsourced clinical development and commercialization services for life sciences
Dublin , GB
https://www.iconplc.com/services/strategic-solutions/
10001+ employees
Qualifications
Bachelor's degree in a scientific or healthcare-related field
Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience
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
should possess a valid driver's license
Employment with ICON is contingent upon having the legal right to work in the country where the role is based
Should possess a valid driver's license
Required skills
Clinical Trial Processes, Onsite Clinical Monitoring, ICH-GCP Guidelines, Clinical Trial Regulations
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