
Clinical Research Associate
1 dia atrás
Clinical Research Associates play a vital role in ensuring the success of clinical trials. As a key member of our team, you will be responsible for coordinating all aspects of site management, from initiation to close-out. Your expertise will help us maintain high-quality standards and ensure compliance with regulatory guidelines.
About ICON Strategic Solutions
We are a leading provider of clinical research services, dedicated to delivering innovative solutions that improve patient outcomes. Our diverse team of professionals is passionate about making a difference in the lives of patients worldwide.
Your Key Responsibilities
* Coordinate site initiation, routine monitoring, and close-out visits
* Ensure sites adhere to GCP/ICH practices and maintain quality of study conduct
* Collaborate with cross-functional teams to resolve issues and address concerns
* Develop and maintain strong relationships with investigators and site staff
Requirements
* Bachelor's degree (or equivalent) with 2 years of independent monitoring experience in Oncology, preferably hematology
* Scientific background and proficiency in medical terminology
* Working knowledge of local regulations and ICH/GCP guidelines
* Excellent record-keeping skills and attention to detail
* Fluency in English, both written and oral
What We Offer
* Competitive salary and benefits package
* Opportunity to work with a diverse team of professionals
* Chance to make a meaningful contribution to the field of clinical research
* Professional development and growth opportunities
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