Clinical Research Associate ICON - Clinical Trial Monitoring
Overview
Design and analyze clinical trials while ensuring protocol compliance and data integrity as a Clinical Research Associate at ICON. This role involves leading monitoring activities and contributing to innovative treatment advancements. The position requires a focus on delivering high-quality clinical data and supporting study documentation.
What You'll Do5
- 1Conduct site qualification initiation monitoring and close-out visits for clinical trials
- 2Ensure protocol compliance data integrity and patient safety throughout the trial process
- 3Collaborate with investigators and site staff to facilitate smooth study conduct
- 4Perform data review and resolve queries to maintain high-quality clinical data
- 5Prepare and review study documentation including protocols and clinical study reports
Requirements5
- 1Bachelor's degree in a scientific or healthcare-related field
- 2Minimum of 2 years of experience as a Clinical Research Associate
- 3In-depth knowledge of clinical trial processes regulations and ICH-GCP guidelines
- 4Strong organizational and communication skills with attention to detail
- 5Ability to work independently and collaboratively in a fast-paced environment
Salary Insight
Salary not disclosed in listing
Location
Required Skills
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