Job Description Join a globally recognized Oncology-focused Pharmaceutical company through your preferred social network. Under the guidance of the Manager, Site Contracts and Budgets, this position is responsible for driving the tactical delivery of assigned studies or programs within the Global Clinical Study Support Department. The role involves participating in project teams to ensure timely contract and budget negotiations, adhering to financial, contractual, and pharmaceutical R&D 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 negotiation and escalation plans. Track progress and status of negotiations, preparing status reports as needed. Facilitate the execution 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 creating, distributing, negotiating, and executing 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. degree, preferably in business, science, healthcare, nursing, or equivalent. At least five (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 processes at relevant organizations. Experience with electronic document management systems or similar portals is preferred. J-18808-Ljbffr