Associate Clinical Operations Manager - Italy

26 ott - Varese
Iqvia

Overview In this role you accelerate clinical trial start-up by negotiating site agreements and ensuring compliance with sponsor requirements and local regulations. You partner with investigative sites, sponsors, legal teams, and cross-functional stakeholders to meet contracts and timelines. Backed by IQVIA's global infrastructure, you gain sponsor-facing exposure and opportunities for long-term career growth in clinical research.

Retribuzione / Benefits bonuses health benefits welfare benefits Negotiate clinical trial contracts with research sites to ensure timely, compliant, and quality agreements Manage contract changes and additional agreements balancing business needs with regulatory requirements Support contract planning and start-up activities for assigned sponsors, studies, and programs Develop investigator grants, site budgets, contracting plans,



and proposal documents Prepare and negotiate contract terms, payment schedules, and budget templates Collaborate with sponsors, stakeholders, and regional start-up teams to achieve project goals Provide contract-related guidance on operational and financial matters to study teams Gather and share contract and market information to support study planning and decision-making Monitor contract activities to meet timelines, milestones, and financial goals Bachelor's degree or equivalent ~3–5 years of experience in clinical research contract management or similar role ~ Familiarity with clinical trial processes, regulatory requirements, and contract lifecycle management ~ Contract management ~ Contract lifecycle management

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