Site Contract Specialist

Job Description Join a global pharmaceutical company focused on oncology. Under the guidance of the Manager, Site Contracts and Budgets, this position is responsible for 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 industry 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 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 training and addressing project questions or issues. Collaborate with study teams to set up and maintain contract management systems for document creation, distribution, negotiation, and execution. Serve as the primary contact and escalation point for investigator sites, global negotiation networks, or study team members during contract negotiations. Assist in preparing performance metrics, such as median cycle times. Notify management of any out-of-scope requests, timeline changes, or resource constraints. Perform other duties as assigned. Requirements B.A./B.S. preferably in a business, science, or healthcare-related field; nursing degree or equivalent preferred. At least five (5) years of experience in a client service role supporting clinical research or healthcare activities within 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 desired. J-18808-Ljbffr

Location: salerno, IT

Posted Date: 5/12/2025