Senior Clinical Research Associate

ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster. The company is seeking a Senior Clinical Research Associate or Clinical Research Associate II to conduct and monitor clinical trials, ensure protocol compliance and data integrity, collaborate with research sites, and support 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

• 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, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
• Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and 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 valid driver's license
• Employment with ICON is contingent upon having the legal right to work in the country where the role is based
• A valid driver's license
• Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.

Required skills

• Clinical Trial Processes, Clinical Trial Regulations, ICH-GCP Guidelines, Independent Clinical Trial Monitoring, Clinical Research

Experience

• 3+ years