Clinical Research Associate II

Accountabilities:: Conduct and document all types of on-site clinical monitoring visits, ensuring study activities meet applicable quality standards and requirements. Participate in study startup activities and feasibility research to support effective site selection and study preparation. Perform Case Report Form (CRF) reviews, source document verification, and clinical data query resolution. Manage site communications and relationships, maintaining effective coordination with investigators and site personnel. Serve as a point of contact for internal support services and external vendors, helping address study-related needs. Communicate regularly with internal project teams regarding site activities, study progress, and relevant issues. Collaborate with regulatory teams to prepare and gather documentation required for clinical study submissions. Support the consistent and timely execution of clinical research activities across assigned studies and therapeutic indications. Requirements: College or university degree in Life Sciences, or an equivalent combination of education, training, and professional experience. Independent on-site clinical monitoring experience in Argentina, as specified in the original posting. Experience conducting all types of monitoring visits for Phase II and/or Phase III clinical trials. Full professional working proficiency in both English and Spanish. Proficiency in Microsoft Office applications. Strong planning and organizational skills, with the ability to manage responsibilities in a dynamic team environment. Effective communication and collaboration skills, with the ability to work with clinical sites, internal teams, and external partners. Strong analytical thinking and problem-solving abilities. Willingness and availability to travel as required by clinical study activities. Experience in oncology is preferred. Benefits: Opportunity to develop clinical research skills through involvement in a variety of monitoring activities. Exposure to clinical studies across different therapeutic indications. Opportunity to broaden therapeutic area knowledge and build expertise in clinical research. Professional development within an established clinical research environment that emphasizes quality and timely delivery.