Job Description: Clinical Contract Specialist Join a leading oncology-focused global pharmaceutical company. Under the guidance of the Manager, Site Contracts and Budgets, this position is responsible for executing the tactical delivery of assigned studies or programs within the Global Clinical Study Support Department. You will participate in project teams to negotiate contracts and budgets, ensuring timely delivery in compliance with industry standards and regulations. Duties and Responsibilities Develop site-specific Confidential Disclosure Agreements (CDAs), Clinical Trial Agreements (CTAs), and other contractual documents. Negotiate contractual documents according to established plans and escalate issues as needed. Track negotiation progress and prepare status reports. Facilitate the signing of contractual documents between investigators, sites, and clients. Mentor new or junior staff, providing project-specific training and support. Collaborate with study teams to manage contract systems for document creation, distribution, negotiation, and execution. Act as the primary contact and escalation point during negotiations. Assist in preparing performance metrics such as median cycle times. Report out-of-scope requests, timeline changes, or resource issues to management. Perform other duties as assigned. Requirements B.A./B.S. in business, science, healthcare, nursing, or equivalent. At least 5 years of experience in a client service role supporting clinical research or healthcare within biotech, pharma, CRO, or related organizations. Experience with Study Start-Up processes in a relevant setting. Familiarity with electronic document management systems or similar portals is preferred. J-18808-Ljbffr