Full-time
Clinical Research Associate
Competitive
Sheetal Champaneria, CCRP & 4 connectionsScience & PharmaceuticalPosted 20d ago
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Role overview
Job type
Salary
Competitive
Sector
Posted
20 days ago
Job description
ICON Strategic Solutions is hiring a sponsor-dedicated Clinical Research Associate to support a client’s cardiovascular and obesity trials. The role monitors clinical trials, ensuring protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff.
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
Remote work arrangement
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 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, ICH-GCP, Clinical Trial Regulations
Experience
2+ years
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