Senior Site Contracts Associate, Iqvia Biotech - Italy

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/83lgfo

In this Senior Site Contracts role, you’ll own contract strategy and start-up contracting for selected sponsors, enabling complex studies and multi‑protocol programs. You’ll work with sponsors, RSU regional teams, and internal partners to ensure timely, compliant, and high-quality contracting. The role combines legal, operational, and financial expertise to drive efficient study start-ups and credible contracting metrics. This position offers line-management opportunities and a chance to influence contracting strategy at scale.Se sta pensando di inviare una candidatura, si ricordi di premere il pulsante apposito dopo aver letto l'intera descrizione.growth-orientedcareer progressionglobal program exposurecompetitive base pay rangeDevelop complex investigator grant estimates, contracting strategies, and proposal text to support business developmentCreate and maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multi‑protocol programsCollaborate with sponsors, stakeholders, and RSU regional teams to ensure successful project delivery and sponsor complianceProvide legal, operational, and financial contracting expertise to support site agreements and streamline start-up and maintenancePrepare and review scientific, technical, and administrative documentation for study initiationAnalyze contracting landscape and disseminate contracting intelligence across the companyEnsure contracting efficiency, timelines,



and achievement of financial targetsTrack and report contracting performance metrics and out‑of‑scope activitiesPartner with Quality Management to uphold high contract management standardsMentor and coach colleagues with training and technical guidancePresent to clients and professional bodies as neededMaintain accurate internal documentation (CTMS, trackers, project plans)Build and maintain relationships with key accounts and preferred clientsBachelor’s degree in related field5+ years of site contracting experience within a sponsor or CROInternational contract expert experienceStrong negotiation and communication skillsExcellent interpersonal skills and experience working in matrix teamsAdvanced legal, financial, and technical writing abilitiesSolid understanding of clinical trial regulations (GCP/ICH) and drug developmentKnowledge xysqume of local and global regulatory requirements, SOPs, and corporate standardsIndependent judgment and ability to take calculated risksStrong project leadership and mentoring experienceExcellent planning, organizational, and presentation skillsProficiency in Microsoft Word, Excel, and Office toolsDeep knowledge of clinical trial contract management processesExperience using metrics to drive timelines and deliverablesAbility to drive programs across departmentsNegotiationCommunicationInterpersonal skillsContract managementRegulatory knowledge (GCP/ICH)Legal writingSenior Site Contracts Associate, IQVIA Biotech - Italy monza-brianza, lombardia, it#J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/83lgfo