Job DescriptionJoin a leading oncology-focused global pharmaceutical company. 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, aligning with financial, contractual, and pharmaceutical RD standards and regulations.Duties and ResponsibilitiesDevelop site-specific Confidential Disclosure Agreements (CDAs), Clinical Trial Agreements (CTAs), or other related contractual documents.Negotiate contractual documents following established plans.Track progress and prepare status reports on contractual negotiations.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 management 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.RequirementsB.A./B.S., preferably in business, science, healthcare, nursing, or an equivalent degree.At least five (5) years of experience in a client service role within biotechnology, pharmaceutical, CRO, or healthcare organizations supporting clinical research.Experience with Study Start-Up processes at relevant organizations.Experience with electronic document management systems or similar portals is desirable.
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