.When our values align, there's no limit to what we can achieve.Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments.From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.We are currently looking for a Global Site Contract Lead based in Hungary, Poland, Romania, Spain, South Africa, Israel, Italy, and the UK.Main Responsibilities:Negotiate study specific generic and country Clinical Site Agreement (CSA) templates with the Sponsor.Support the PL in the negotiation of country budgets with the Sponsor.Provide the local CTS / CRA with required CSA country templates.Manage CSA activities and liaise with PL, GRO Lead, and the Sponsor to ensure that CSA start-up deliverables are met.Key Accountabilities:Act as functional Specialist on projects and develop study specific CSA strategy.Agree and negotiate study specific generic and country CSA templates with the Sponsor.Gather relevant study information from PL.Discuss and finalize specific country CSA templates with input from Sponsor, PL, and GRO Lead if appropriate.Store the final approved and complete country template and country budget PMED.Communicate CSA strategy, CSA turnaround timelines, CTMS tracking requirements, and budget information/updates with the assigned CTS/CRAs.Provide agreed study and country CSA templates to local CTS/CRA for country specific adaptation.Coordinate interaction between GRO Lead, PL, and Sponsor including overall timeline management for CSAs.Coordinate overall CSA process with assigned CTS/CRA and status reporting to GRO-Lead/PL.Provide updates about template amendments, process changes, investigator fees, local requirements etc. to ensure that relevant CSA database is up-to-date.Maintain comprehensive language tracker.Early recognition of areas of potential problems and formulate contingency plans.Define solutions strategy of significant CSA changes requested by the site.Evaluate and identify resourcing needs of SSU staff to be assigned on the project and provide performance feedback as appropriate.Participate in client, investigator, and team meetings.Identify and facilitate CSA training needs of local CTS/CRA.Maintain and assure quality of work generated.Compile CSA status within a project as agreed with PL and GRO Lead.Prioritize effectively and respond to urgent requests within team or sponsor lead.Provide mentoring and coaching to CTS staff.Resolve negotiation issues that have arisen at the clinical site and escalated from the CTS.Escalate changes that fall outside the documented fall-back parameters to the Sponsor or to Clinical Site Agreement Manager as appropriate