As a Clinical Research Associate, you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will be part of an innovative and global Biotechnology company, which prides itself on being one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today. What you will be doing: Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance with applicable regulations. Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and SOPs. Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. Participates in audit preparation and follow-up activities as needed. May serve as preceptor, providing training to less experienced clinical team members. May be assigned clinical tasks where advanced negotiating skills are required. You are: Bachelor's degree in a health, life sciences, or other relevant field of study. Previous experience supporting clinical trials including 2 years of on-site monitoring experience. Previous experience in oncology is a plus. Travel is required. All employees must read, write, and speak fluent English and host country language. * Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. #J-18808-Ljbffr