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Clinical Research Associate Professional
1 week ago
We are a leading clinical research organization that delivers innovative solutions to improve patient outcomes. Our team is passionate about advancing medical knowledge and driving healthcare progress.
As a Clinical Research Associate, you will play a critical role in ensuring the success of our clinical trials. Your expertise will be instrumental in conducting site qualification, initiation, monitoring, and close-out visits. You will work closely with investigators and site staff to facilitate smooth study conduct, ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Key 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
Requirements:
- Bachelor's degree in a scientific or healthcare-related field highly preferred
- Minimum of 2 years of experience as a Clinical Research Associate (on-site monitoring experience required)
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Our Culture:
We value diversity, inclusion, and belonging at ICON Clinical Research. Our team is committed to fostering an environment where everyone can thrive. We offer competitive benefits, including health insurance options, retirement planning, and flexible work arrangements.