Overview Senior Contract Associate (sponsor-dedicated role). You will oversee the preparation, negotiation, and finalisation of clinical trial agreements and budgets in compliance with FMV, legal, and regulatory requirements. You will act as the primary liaison with sites and internal stakeholders while managing timelines, maintaining accurate tracking, and supporting contract amendments and template updates. Essential Functions Develop and coordinate the development of investigator grants and estimates, contracting strategies, and proposal text to support the proposal development process. Develop contract language, payment language, and budget templates as required for the position. Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies, or multi-protocol programs according to the Scope of Work and Project Plan within the agreed project strategy. Ensure collaboration with sponsors, stakeholders, and RSU regions and countries as applicable to the position to deliver the project scope in compliance with sponsor requirements and the RSU Management Plan. Provide specialist legal, operational, and financial contracting support to Study Teams for site agreements to facilitate business development, initiation, and maintenance of clinical trials while ensuring regulatory compliance. Assist with the creation and/or review of core scientific, technical, and administrative documentation to support business development and enable study initiation and maintenance. Contribute to the collection, interpretation, analysis, and dissemination of contracting intelligence to support assigned studies and the wider company. Ensure contracting efficiency and adherence to project timelines and financial goals for site agreements. Report contracting performance metrics and out-of-scope contracting activities as required. Work with Quality Management to ensure appropriate contract management and quality standards; mentor and coach colleagues and deliver training materials as required. Deliver presentations to clients as required and ensure accurate completion and maintenance of internal systems (including CTMS), databases, tracking tools, timelines, and project plans. May take a proactive role in developing long-standing relationships with preferred IQVIA clients/customers. Qualifications Bachelor's Degree in a Related Field 5 years of relevant sponsor or clinical research organization contract contracting experience, including demonstrable global and/or regional experience acting as a contract negotiator. IQVIA is an equal opportunity employer. All information provided in your application must be truthful and complete. False statements may lead to disqualification or termination in accordance with applicable law. #J-18808-Ljbffr