PAs Clinical Site Manager you will be responsible for maximizing site performance and site engagement in our client conducted clinical studies, as well as leveraging strong clinical operational and therapeutic expertise to support execution of the clinical studies. /ppICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. /ppbWhat you will be doing : /b /pulliResponsible for the planning, initiation, coordination and management of all monitoring and monitoring-related activities as well as supervision of all site-related activities to ensure compliance with the client Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory requirements /liliEngage with clinical sites to develop, build, and maintain strong relationships with investigators / staff that will ensure high quality investigative sites to support the client’s clinical development programs /liliCollaborate with internal and external stakeholders as well as third party vendors /liliProvide operational support to the CPM / Sr CPM to deliver the study within planned timelines and according to required standards of quality and compliance /liliEvaluate, screen and develop high quality investigative sites to support the client’s clinical development programs /liliResponsible for the early engagement with Key Opinion Leaders (KOLs) / sites / patients organizations and key contact point for these throughout the study. /liliInteract / train new investigators to work on the client clinical trials /liliAttend key therapeutic trainings / meetings and / or industry trainings /li /ulpbYou are : /b /pulliA SCRA with a minimum of 4+ years of monitoring experience in Italy /liliExcellent verbal and written communication in local language and English /liliOperate effectively within an international and rapidly changing environment /liliAbility to supervise monitoring and related activities in a clinical trial /liliAbility to have scientific discussions with Investigators and Site Personnel /liliBA / BS Degree required /liliAbility to travel domestically /li /ulpbWhat ICON can offer you : /b /ppOur 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. /ppIn 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. /pulliVarious annual leave entitlements /liliA range of health insurance offerings to suit you and your family’s needs /liliCompetitive retirement planning offerings to maximise savings and plan with confidence for the years ahead /liliGlobal 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-being /liliLife assurance /liliFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others /li /ulpVisit 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. /ppin 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. /ppJ-18808-Ljbffr /ppJ-18808-Ljbffr /p #J-18808-Ljbffr