pMilan, Italy /p pFull time /p pR /p pbSr. Site Contracts Associate /b /p pbIQVIA Biotech /b /p pbItaly - Homebased /b /p pIQVIA 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. /p h3? Overview /h3 pWe are seeking an experienced bSenior Site Contracts Associate /b 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. /p pIf you are a strategic thinker with strong expertise in international clinical trial contracting, we’d love to speak with you. /p h3? Key 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 h3? Qualifications Experience /h3 ul liBachelor’s degree in a related field (required). /li lib5+ years of site contracting experience /b 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 h3? What 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 /p pIQVIA 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, 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. 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 part‑time). 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 pIQVIA 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. Everything we do is part of a journey to improve patient outcomes and population health worldwide. /p pTo get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. /p pEEO Minorities/Females/Protected Veterans/Disabled /p #J-18808-Ljbffr

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