Study Start Up Associate

Study Start Up Associate (Level I, II or Senior) - Contracts and budgets - Homebased - BrazilICON 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 developmentWe are currently seeking a Study Start Up Associate I, II or Senior to join our diverse and dynamic team. As a Study Start Up Associate at ICON, you will be responsible for the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, budgets and other ancillary agreements with investigative sites.What you will be doing- Draft, review, negotiate, and finalize clinical trial agreements, complex amendments, budgets and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON’s fundamental interests and is consistent with ICON’s rules, procedures, and policies.- Maintain consistent communication with sponsor, study sites and internal stakeholders in alignment with site contracts and budget department and client requirements.- Track progress of site contracts and budget agreements and related documents regularly in required ICON and client systems.- Proactively identify and raise risks, while also, suggesting mitigation plans to established study milestones and planned site contracts timelines.- File contractual documents per department, ICON, and client requirements.- Work cross functionally with sponsor and internal stakeholders in support of timely site start up and maintenance for the conduct of clinical trials including accurate forecast of contract and budget execution timelines.- Review site budgets and contracts for completeness and accuracy and ensure adherence to department and client requirements, corrects documents, and files changes to contracts.- Participate/contribute in departmental initiatives.- May serve as mentor for other site contracts department team members.- Complete all required project, client, department, and ICON trainings on time and adheres to the applicable SOPs, processes, and procedures.Your profile- 1+ years of relevant clinical research and site contracts and budgets experience.- Bachelors Degree.- Experience in dealing with external and internal clients.-- Ability to follow written and oral instructions from a variety of sources.- Ability to mentor and train other site contracts team members as needed.- Effective time management skills and ability to prioritize multiple tasks with mínimal management guidance and oversight.- Strong attention to detail.- Great interpersonal and communication skills.- Fluent in EnglishLI-FB2LI-RemoteWhat 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 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 assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit ourcareers siteto read more about the benefits ICON offers.