h3Questa posizione è in IQVIA /h3 pIl processo di selezione sarà interamente gestito IQVIA. /p h3Sr. Site Contracts Associate IQVIA Biotech Italy - Homebased IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster. /h3 h3Overview /h3 pWe 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. /p h3Key Responsibilities /h3 ul liDevelop complex investigator grant estimates, contracting strategies, and proposal text to support business development. /li liCreate and maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multi-protocol programs. /li liCollaborate closely with sponsors, stakeholders, and RSU regional teams to ensure successful delivery of the project scope and compliance with sponsor requirements. /li liProvide legal, operational, and financial contracting expertise to support site agreements and facilitate efficient study start-up and maintenance. /li liCreate and review scientific, technical, and administrative documentation required for study initiation. /li liAssess the contracting landscape and contribute to the analysis and dissemination of contracting intelligence across the company. /li liEnsure contracting efficiency, adherence to timelines, and achievement of financial targets.



/li liTrack and report contracting performance metrics and out-of-scope activities. /li liPartner with Quality Management to uphold high contract management and quality standards. /li liMentor and coach colleagues, delivering training and technical guidance. /li liPresent to clients and professional bodies as needed. /li liMaintain accurate internal system documentation, including CTMS, trackers, and project plans. /li liBuild and maintain strong relationships with preferred clients, serving as liaison for key accounts when required. /li /ul h3Qualifications Experience /h3 ul liBachelor’s degree in a related field (required). /li li5+ years of site contracting experience within a sponsor or CRO, including demonstrable experience as an international contract expert. /li liEquivalent combinations of education, training, and experience will be considered. /li liStrong negotiation and communication skills, with the ability to challenge and influence. /li liExcellent interpersonal skills and proven success working within matrix teams. /li liAdvanced legal, financial, and technical writing abilities. /li liSolid understanding of clinical trial regulations, GCP/ICH, and the overall drug development process. /li liKnowledge of local and global regulatory requirements, SOPs, and corporate standards. /li liAbility to exercise independent judgment and take calculated risks. /li liStrong project leadership skills and experience mentoring others. /li liExcellent planning, organizational, and presentation skills. /li liStrong proficiency in Microsoft Word, Excel, and other Office tools.



/li liDeep knowledge of clinical trial contract management processes. /li liProven experience leveraging metrics to establish timelines and deliverables. /li liAbility to initiate and grow programs across departments to drive organizational impact. /li /ul h3What We Offer /h3 ul liOpportunity to work on global, high-complexity clinical programs. /li liA collaborative, supportive, and growth-oriented environment. /li liThe chance to influence key clients and shape contracting strategy at scale. /li liCareer progression and professional development opportunities. /li /ul pIQVIA 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. Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentation, 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. We appreciate your honesty and professionalism. /p pThe potential base pay range for this role, when annualized, is €41,000.00 - €79,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or tempo parziale). Dependent 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. /p #J-18808-Ljbffr

📌 Senior Site Contracts Associate, IQVIA Biotech - Italy (Italia)
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