ppIn 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. /p /brul /brligrowth-oriented /li /brlicareer progression /li /brliglobal program exposure /li /brlicompetitive base pay range /li /brliDevelop complex investigator grant estimates, contracting strategies, and proposal text to support business development /li /brliCreate and maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multi‑protocol programs /li /brliCollaborate with sponsors, stakeholders, and RSU regional teams to ensure successful project delivery and sponsor compliance /li /brliProvide legal, operational, and financial contracting expertise to support site agreements and streamline start-up and maintenance /li /brliPrepare and review scientific, technical, and administrative documentation for study initiation /li /brliAnalyze contracting landscape and disseminate contracting intelligence across the company /li /brliEnsure contracting efficiency, timelines,



and achievement of financial targets /li /brliTrack and report contracting performance metrics and out‑of‑scope activities /li /brliPartner with Quality Management to uphold high contract management standards /li /brliMentor and coach colleagues with training and technical guidance /li /brliPresent to clients and professional bodies as needed /li /brliMaintain accurate internal documentation (CTMS, trackers, project plans) /li /brliBuild and maintain relationships with key accounts and preferred clients /li /brliBachelor’s degree in related field /li /brli5+ years of site contracting experience within a sponsor or CRO /li /brliInternational contract expert experience /li /brliStrong negotiation and communication skills /li /brliExcellent interpersonal skills and experience working in matrix teams /li /brliAdvanced legal, financial, and technical writing abilities /li /brliSolid understanding of clinical trial regulations (GCP/ICH) and drug development /li /brliKnowledge of local and global regulatory requirements, SOPs, and corporate standards /li /brliIndependent judgment and ability to take calculated risks /li /brliStrong project leadership and mentoring experience /li /brliExcellent planning, organizational, and presentation skills /li /brliProficiency in Microsoft Word, Excel, and Office tools /li /brliDeep knowledge of clinical trial contract management processes /li /brliExperience using metrics to drive timelines and deliverables /li /brliAbility to drive programs across departments /li /brliNegotiation /li /brliCommunication /li /brliInterpersonal skills /li /brliContract management /li /brliRegulatory knowledge (GCP/ICH) /li /brliLegal writing /li /br /ul /brpSenior Site Contracts Associate, IQVIA Biotech - Italy monza-brianza, lombardia, it /p /p #J-18808-Ljbffr

📌 Senior Site Contracts Associate, Iqvia Biotech - Italy (Monza)
🏢 Iqvia
📍 Monza