Clinical Research Associate
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Job Description
Clinical Research Associate monitoring early-development clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Conducting site visits, ensuring ICH-GCP compliance, and maintaining data integrity and patient safety.
Responsibilities:
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolve queries to maintain high-quality clinical data
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports
- Take responsibility for deliverables and work collaboratively on clinical trial monitoring activities
Requirements:
- 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
- Willingness to travel as required, approximately 60%
- Legal right to work in the United States
Benefits:
- Competitive base salary and performance related incentives
- 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
- Inclusive and accessible workplace
- Reasonable accommodations during the recruitment process
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