Job Description

Overview: The Clinical Trial Operations Associate supports the setup and management of clinical studies, focusing on financial and contractual aspects. This role ensures that investigator sites are equipped to enrol study participants by managing site budgets, negotiating and finalizing contracts, and maintaining compliance throughout the study lifecycle, from start-up to close-out. The position also contributes to clinical finance, documentation management, and inspection readiness, ensuring that records are complete, accurate, and accessible. *Fluency in German and Italian is required* Key Responsibilities Lead investigator site start-up activities, including the collection and submission of regulatory documentation Customize, review, and negotiate informed consent documents in collaboration with internal and external stakeholders Act as the primary point of contact for site Ethics Review Boards (ERBs) and Competent Authorities (CAs), where applicable Manage site budget discussions a...

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