Clinical Research Associate
4 weken geleden
ICON plc is a world-leading healthcare intelligence and clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations. Our mission is to accelerate the development of drugs and devices that save lives and improve quality of life.
We are seeking an experienced Clinical Research Associate based in the Netherlands to join our team. As a CRA, you will work independently to set up and monitor studies, complete reports, and maintain documentation. You will also be responsible for submitting protocol and consent documents for ethics/IRB approval and preparing regulatory submissions.
The ideal candidate will have 3+ years of monitoring experience in phase I-III trials as a CRA, a college degree in medicine, science, or equivalent, and knowledge of ICH-GCP guidelines. You will also have excellent written and verbal communication skills and the ability to work to tight deadlines.
We offer a comprehensive and competitive total reward package, including a wide range of variable pay and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career.
At ICON, we are committed to developing our employees in a continuous learning culture. We challenge you with engaging work and every experience adds to your professional development.
We are an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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