OverviewIn 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. You mitigate risk, resolve contractual issues, and drive timely site activation. Backed by IQVIA's global infrastructure, you gain sponsor-facing exposure and opportunities for long-term career growth in clinical research.Retribuzione / Benefitsincentive plansbonuseshealth benefitswelfare benefitsResponsabilitàNegotiate clinical trial contracts with research sites to ensure timely, compliant, and quality agreementsManage contract changes and additional agreements balancing business needs with regulatory requirementsSupport contract planning and start-up activities for assigned sponsors, studies, and programsDevelop investigator grants, site budgets, contracting plans, and proposal documentsPrepare and negotiate contract terms,
payment schedules, and budget templatesCollaborate with sponsors, stakeholders, and regional start-up teams to achieve project goalsProvide contract-related guidance on operational and financial matters to study teamsGather and share contract and market information to support study planning and decision-makingMonitor contract activities to meet timelines, milestones, and financial goalsRequisiti fondamentaliBachelor's degree or equivalent3–5 years of experience in clinical research contract management or similar roleFamiliarity with clinical trial processes, regulatory requirements, and contract lifecycle managementStrong analytical, organizational, and communication skillsAnalytical mindsetStrong communicationOrganizational skillsContract managementRegulatory knowledgeContract lifecycle management
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