Senior Site Contracts Associate, IQVIA Biotech - Italy
Pubblicato il 06-10-2026 - Iqvia in Italia
h3Sr. Site Contracts Associate IQVIA Biotech Italy - Homebased /h3h3Overview /h3pWe are seeking an experienced Senior Site Contracts Associate to manage contract strategy and oversee all start‑up contracting activities for selected sponsors. In this role, you will support complex studies and multi‑protocol programs, ensuring high‑quality delivery and operational excellence. This position may also include line‑management responsibilities. If you are a strategic thinker with strong expertise in international clinical trial contracting, we’d love to speak with you. /ph3Key Responsibilities /h3ulliDevelop complex investigator grant estimates, contracting strategies, and proposal text to support business development. /liliCreate and maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multi‑protocol programs. /liliCollaborate closely with sponsors, stakeholders, and RSU regional teams to ensure successful delivery of the project scope and compliance with sponsor requirements. /liliProvide legal, operational, and financial contracting expertise to support site agreements and facilitate efficient study start‑up and maintenance. /liliCreate and review scientific, technical, and administrative documentation required for study initiation. /liliAssess the contracting landscape and contribute to the analysis and dissemination of contracting intelligence across the company. /liliEnsure contracting efficiency, adherence to timelines, and achievement of financial targets. /liliTrack and report contracting performance metrics and out‑of‑scope activities. /liliPartner with Quality Management to uphold high contract management and quality standards. /liliMentor and coach colleagues, delivering training and technical guidance. /liliPresent to clients and professional bodies as needed. /liliMaintain accurate internal system documentation, including CTMS, trackers, and project plans.
/liliBuild and maintain strong relationships with preferred clients, serving as liaison for key accounts when required. /li /ulh3Qualifications Experience /h3ulliBachelor’s degree in a related field (required). /lili5+ years of site contracting experience within a sponsor or CRO, including demonstrable experience as an international contract expert. /liliEquivalent combinations of education, training, and experience will be considered. /liliStrong negotiation and communication skills, with the ability to challenge and influence. /liliExcellent interpersonal skills and proven success working within matrix teams. /liliAdvanced legal, financial, and technical writing abilities. /liliSolid understanding of clinical trial regulations, GCP/ICH, and the overall drug development process. /liliKnowledge of local and global regulatory requirements, SOPs, and corporate standards. /liliAbility to exercise independent judgement and take calculated risks. /liliStrong project leadership skills and experience mentoring others. /liliExcellent planning, organizational, and presentation skills. /liliStrong proficiency in Microsoft Word, Excel, and other Office tools. /liliDeep knowledge of clinical trial contract management processes. /liliProven experience leveraging metrics to establish timelines and deliverables. /liliAbility to initiate and grow programs across departments to drive organizational impact. /li /ulh3What We Offer /h3ulliOpportunity to work on global, high‑complexity clinical programs. /liliA collaborative, supportive,
and growth‑oriented environment. /liliThe chance to influence key clients and shape contracting strategy at scale. /liliCareer progression and professional development opportunities. /liliDependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. /li /ulpThe potential base pay range for this role, when annualized, is €41,000.00 - €79,800.00. /ppIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. /ppLearn more at /ppIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. /ppEverything we do is part of a journey to improve patient outcomes and population health worldwide. /ppWe appreciate your honesty and professionalism. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. /ppTo get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. /ppNo matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. /ppThank you for your interest in growing your career with us. /p #J-18808-Ljbffr