Clinical Trial Manager (SASM) 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 We are hiring a Clinical Trial Manager in the UK! The role can be fully homebased in the UK and this is a non-travelling position. This is a great opportunity to steer your career towards clinical trial management. It would suit a Junior Clinical Trial Manager or Senior Clinical Project Specialist with solid multiple country exposure, looking for their first clinical trial management position. Global clinical trial experience is essential to succeed! You will be part of an innovative and global Biotechnology company, who pride themselves to be 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 Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials Vendor management and support vendor relationships Work with the clinical trial management staff to support the execution and monitoring of clinical studies and trial deliverables Contribute to and support with the preparation, writing and review of study related documents including but not limited to, clinical protocols, study guides, monitoring plans, e(CRF)s, subject information sheets and consent forms, clinical study report, regulatory submissions and publications Coordinate the activities associated with site start-up and overall trial management Coordinate study level investigational product arrangements, accountability and reconciliation Contribute to, or coordinate preparation and conduct of site initiations, monitors’ workshops (as applicable) and investigator meetings (as applicable) Assists in preparing and managing Study Budgets and timelines Coordinate study level investigational product arrangements and study start-up and management activities Perform protocol-related site management activities What is required BS/BA/BSc in the sciences preferred or RN or above 5 years’ work experience, ideally, in life sciences or medically related field, including 2 years of direct biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company Project Management, project planning experience including oversight of study deliverables, budgets, and timelines Experience interacting with external vendors (CROs, central labs, imaging vendors, etc.) Experience with development of prospective site – selection criteria Risk assessment, management and mitigation; delivery and risk focused Initiative and critical thinking & planning ability Good organization, planning & communication skills What is offered Solid structured on-boarding Full-time and permanent contract of employment with us seconded to one single sponsor Homebased in the UK/England Salary according to level of skills and experience 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. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global 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. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At 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, color, 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. Interested 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. Are you a current ICON Employee? Please click here to apply ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? 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