ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.As a Clinical Research Associate II at ICON, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP.You will be partnering with a pharmaceutical company committed to discovering and developing treatments that improve and save people´s lives. Working in this program you will feel challenged and supported to advance in your professional career while making a truly impact.What you will be doing:Independent, proactive work to set up and monitor studies, complete reports and maintain documentationSubmitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissionsBalancing sponsor generated queriesTaking responsibility for study cost efficiencyPreparation and review of study documentation and feasibility studies for new proposalsPotential to assist in training and mentoring fellow CRAsYou are:Degree in medicine, science, or equivalentPrevious experience in a clinical research setting (e.g., as a Study Coordinator or Clinical Trial Assistant), with a solid understanding of study processes, site coordination, and regulatory requirements (ICH-GCP).Knowledge of ICH-GCP guidelines and ability to review and evaluate medical dataExcellent written and verbal communication in both English and GermanAbility to work to tight deadlinesAvailability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving licenseWhat 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.Our benefits examples include:Various annual leave entitlementsA range of health insurance offerings to suit you and your family's needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among othersVisit our careers website to read more about the benefits of working at ICON: ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 through the form below. in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.#LI-RR1 #J-18808-Ljbffr