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Site contract specialist

Palermo
JR Italy
Pubblicato il Pubblicato 9h fa
Descrizione

Social Network Login/JoinOncology-focused Global Pharmaceutical companyPosition OverviewUnder the guidance of the Manager, Site Contracts and Budgets, this position will be responsible for driving the tactical delivery of assigned studies or programs for the Global Clinical Study Support Department. The role involves participating in project teams to deliver contract and budget negotiations on time, in accordance with applicable financial, contractual, and pharmaceutical RD industry standards and regulations.Duties and ResponsibilitiesDevelop site-specific Confidential Disclosure Agreements (CDAs), Clinical Trial Agreements (CTAs), or other related contractual documents.Negotiate contractual documents using established negotiation and escalation plans.Track the progress and status of contractual negotiations and prepare status reports as required.Facilitate the execution of contractual documents between investigators, sites, and clients.Serve as a mentor to new or junior staff, providing project-specific training and addressing questions/issues.Work collaboratively with the study team to set up and maintain contract management systems for creation, distribution, negotiation, and execution of contractual documents.Serve as the primary contact and escalation point for investigator sites, the global negotiation network, or study team members during contractual negotiations.Assist with preparing performance metrics, such as median cycle times.Notify management of out-of-scope requests, timeline changes, or resource constraints.Perform other duties as assigned.RequirementsB.A./B.S. preferably in a business or science/healthcare field, nursing degree, or equivalent.Minimum of five (5) years of experience in a client service role within a biotechnology or pharmaceutical company, CRO, or similar organization supporting clinical research or healthcare activities.Previous Study Start-Up experience in a related organization.Experience with electronic document management systems or similar portals is desired.
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