Summary: Manage the design and launch of clinical research studies, owning start-up deliverables and ensuring quality execution. Highlights: 1. Manage study database design and configuration for clinical research 2. Act as primary set-up contact for sponsors and internal stakeholders 3. Work in a fast-paced, deadline-driven environment Buenos Aires, Argentina \| Full time \| Hybrid \| R1526663### **We are seeking a Study Start\-Up Project Manager to join IQVIA Laboratories at Buenos Aires.** We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Job Summary: Manage the design and launch of clinical research studies, owning start\-up deliverables and ensuring quality execution across sponsors, CROs, and internal teams. What You’ll Be Doing:* Develop and manage study database design requirements for protocols, amendments, and sponsor changes * Configure and oversee study databases in alignment with clinical protocols and sponsor standards * Act as the primary set\-up point of contact for sponsors and internal stakeholders * Coordinate start\-up activities across Data Management, Logistics, Clinical Trial Materials, Laboratory Testing, and Specimen Management * Maintain and communicate project timelines, action logs, issue logs, and status reports during start\-up * Proactively manage scope changes, identify risks, and implement contingency plans What We Are Looking For:* Bachelor’s degree in science or a related field. * Experience with clinical study database design and configuration * Working knowledge of Clinical Trials Management Systems * Proficiency with Microsoft Office applications * Other Equivalent combination of education, training, and experience may be accepted in lieu of degree The Knowledge, Skills and Abilities Needed for This Role:* Strong understanding of clinical research terminology and ICH E6 Good Clinical Practice guidelines * Excellent organizational, time management, and attention to detail skills * Ability to work effectively in a fast\-paced, deadline\-driven environment What We Offer You: We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of employees’ physical, mental, emotional, financial, and social well\-being. To learn more about our benefits, visit https://jobs.iqvia.com/benefits. If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible! IQVIA 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 https://jobs.iqvia.com 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, 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.