Clinical Research Associate II

📋 Description

• Conduct and document all types of on-site clinical monitoring visits, ensuring study activities
• Participate in study startup activities and feasibility research to support effective site
• Perform Case Report Form (CRF) reviews, source document verification, and clinical data query
• Manage site communications and relationships, maintaining effective coordination with investigators
• Serve as a point of contact for internal support services and external vendors, helping address
• Communicate regularly with internal project teams regarding site activities, study progress, and

🎯 Requirements

• College or university degree in Life Sciences, or an equivalent combination of education, training
• Independent on-site clinical monitoring experience in Argentina, as specified in the original
• 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

🎁 Benefits

• Opportunity to develop clinical research skills through involvement in a variety of monitoring
• 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