Clinical Research Associate 2
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Experteer Overview
As a Clinical Research Associate II, you drive the conduct and oversight of clinical trials across sites. You will monitor study activities, ensure adherence to protocols and patient safety, and collaborate with investigators to maintain data quality.This role supports the advancement of innovative treatments within a diverse, inclusive environment. You will engage across study documentation and data review to enable reliable trial results. This opportunity offers meaningful impact in a fast-paced, globally collaborative setting.
Compensaciones / Beneficios- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout the trial
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolution of queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation, including protocols and clinical study reports
- 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%)
- Annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme LifeWorks
- Life assurance
- Flexible country-specific optional benefits
Icon Clinical PLCMadrid
a Clinical Research Associate with strong understanding of trial processes and regulatory requirements
• Proven ability to manage multiple sites and projects with strong organizational and problem-solving skills
• Expertise in monitoring practices, data...
Icon Clinical PLCMadrid
Research Associate with strong understanding of trial processes and regulatory requirements
• Ability to manage multiple sites and projects simultaneously with strong organizational and problem-solving skills
• Expertise in monitoring practices, data...
Icon Clinical PLCMadrid
Experteer Overview
As a Clinical Research Associate II at ICON, you will support the design, execution, and oversight of clinical trials to advance innovative therapies. You will ensure protocol adherence, data integrity, and patient safety while...