Qureos Mentor

ICON Strategic Solutions

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 ** Must have 2 years of onsite monitoring experience**
 
 
 **Must have Ophthalmology experience**
 
 
 
 
 
 We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
 
 
 
 
 
 
 What you will be doing
 
 
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 Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
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 Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
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 Collaborating with investigators and site staff to facilitate smooth study conduct.
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 Performing data review and resolution of queries to maintain high-quality clinical data.
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 Contributing to the preparation and review of study documentation, including protocols and clinical study reports
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 Your profile
 
 
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 Bachelor's degree in a scientific or healthcare-related field.
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 Minimum of 2 years of experience as a Clinical Research Associate.
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 In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
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 Strong organizational and communication skills, with attention to detail.
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 Ability to work independently and collaboratively in a fast-paced environment.
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 Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver&rsquo;s license
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Clinical Research Associate

Join ICON Strategic Solutions and explore 1   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

ICON Strategic Solutions

About Company

Clinical Research Associate