Job Description Join a global pharmaceutical company focused on oncology. Under the guidance of the Manager, Site Contracts and Budgets, this position will drive the tactical delivery of assigned studies or programs within the Global Clinical Study Support Department. The role involves participating in project teams to deliver contract and budget negotiations on time, adhering to financial, contractual, and pharmaceutical R&D standards and regulations. Duties and Responsibilities Develop site-specific Confidential Disclosure Agreements (CDAs), Clinical Trial Agreements (CTAs), or other related contractual documents. Negotiate contractual documents following established plans. Track progress and status of negotiations; prepare status reports. Facilitate execution of contractual documents between investigators, sites, and clients. Mentor new or junior staff, providing training and addressing project questions. Collaborate with study teams to manage contract systems for creation, distribution, negotiation, and execution of documents. Serve as the primary contact and escalation point during negotiations. Assist in preparing performance metrics, such as median cycle times. Notify management of out-of-scope requests, timeline changes, or resource issues. Perform other duties as assigned. Requirements B.A./B.S. in business, science, healthcare, nursing, or an equivalent degree. At least five (5) years of experience in a client service role supporting clinical research or healthcare activities in biotech, pharma, CRO, or related organizations. Experience with Study Start-Up processes at relevant organizations. Experience with electronic document management systems or similar portals is preferred. J-18808-Ljbffr