ph3Senior Study Start Up Associate - Hybrid - Romania /h3 pICON 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. /p pAs a Principal Study Start-Up Associate at ICON, you will be responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals. /p h3What You Will Do: /h3 pYour focus will be execution and oversight of clinical trial country submissions and approvals and negotiations of budgets and CTAs with sites. /p pKey responsibilities include: /p ul liLead the negotiation and execution of Clinical Trial Agreements (CTAs), including site contracts and budget negotiations, ensuring timely study start-up. /li liManage and oversee clinical trial payments throughout the study lifecycle, including payment tracking, issue resolution, and close-out reconciliation. /li liPrepare, review, and submit essential regulatory and site documentation to support approvals and successful site activation. /li liPartner with local study teams and investigative sites to drive start-up activities and ensure milestones are achieved on schedule. /li liProvide expert guidance on study start-up processes, requirements, and best practices, fostering strong collaboration and communication among stakeholders. /li /ul h3Your Profile: /h3 pYou will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team. /p h3Required qualifications and experience: /h3 ul liBachelor's degree in Life Sciences, Healthcare,



or a related scientific discipline. /li liComfortable working in a hybrid environment, with the flexibility to attend the office 1-3 days per week. /li liStrong knowledge of site budget development, contract negotiations, and local regulatory requirements, including submission and approval processes. /li liProven experience in clinical study start-up activities, with a solid understanding of regulatory frameworks and site activation requirements. /li liExperience managing clinical trial site payments and payment reconciliation processes. /li liExcellent organizational skills with a strong attention to detail and the ability to manage multiple priorities effectively. /li liStrong verbal and written communication skills /li /ul h3What ICON can offer you: /h3 pOur 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. /p pIn 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. /p h3Our benefits examples include:



/h3 ul liVarious annual leave entitlements /li liA range of health insurance offerings to suit you and your family's needs. /li liCompetitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. /li liGlobal Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. /li liLife assurance /li liFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. /li /ul pVisit our careers site ( to read more about the benefits ICON offers. /p pAt 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. /p pIf, 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 ( /p pInterested 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. /p /p #J-18808-Ljbffr

📌 Principal Study Start-Up Associate (Roma)
🏢 Icon Clinical Research
📍 Roma