Summary: Perform country-level site activation activities, manage regulatory documents, and support internal systems for clinical trials. Highlights: 1. Perform site activation activities in assigned studies 2. Review and track regulatory, ethics, and ICF documents 3. Support updating and maintenance of internal systems and project plans Buenos Aires, Argentina \| Full time \| Hybrid \| R1520481 **Site Activation Coordinator****Job Overview** Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.**Essential Functions** * Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff. * Prepare site regulatory documents, reviewing for completeness and accuracy. * Inform team members of completion of regulatory and contractual documents for individual sites. * Distribute completed documents to sites and internal project team members. * Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information. * Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. **Qualifications** * Bachelor's Degree Life sciences or a related field . * 1 years’ experience in a healthcare environment or equivalent combination of education, training and experience. * Advanced English level * Good interpersonal communication and organizational skills. * Good attention to detail. * General awareness clinical trial environment and drug development process. * Ability to work on multiple projects. * Ability to establish and maintain effective working relationships with co\-workers, managers and sponsors. 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.