Social Network Login/Join Join or login with your social network account. Position Overview We are an oncology-focused global pharmaceutical company seeking a dedicated professional to support our Global Clinical Study Support Department. Under the guidance of the Manager, Site Contracts and Budgets, this role involves driving the tactical delivery of assigned studies or programs, participating in project teams to negotiate contracts and budgets 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 following established plans and escalate as needed. Track negotiation progress and prepare status reports. Facilitate the execution of contractual documents between investigators, sites, and clients. Mentor and train new or junior staff on project-specific tasks. Collaborate with study teams to manage contract systems for document creation, distribution, negotiation, and execution. 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., preferably in business, science, healthcare, nursing, or an equivalent degree. At least 5 years of experience in a client service role within biotechnology, pharmaceuticals, CROs, or related healthcare organizations supporting clinical research. Experience with study start-up activities at relevant organizations. Experience with electronic document management systems or similar portals is preferred. J-18808-Ljbffr