Worldwide Clinical Trials seeks a Clinical Trials Associate to provide administrative and project-tracking support for clinical research teams across Argentina, Mexico, and Brazil. The role involves managing documentation, system access, training coordination, and meeting logistics to ensure timely study delivery and regulatory compliance.
Responsibilities
Coordinate system access and permissions for project team members
Maintain project portals and verify accuracy of current document versions
Prepare, track, and file clinical trial documentation including Investigator Site Files
Prepare and distribute meeting minutes and track project information logs
Coordinate project-specific training schedules and participant updates
Requirements
Bachelor's degree or equivalent professional experience
Minimum one year in clinical operations or related administrative role
Fluent English (written and verbal) plus local language proficiency
Knowledge of ICH, GCP, and FDA or EU regulatory requirements
Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint)
Strong organizational and attention-to-detail skills
Ability to manage multiple priorities independently and collaboratively

📌 Clinical Trials Associate - Argentina - Mexico - Brazil (Buenos Aires)
🏢 Worldwide Clinical Trials
📍 Buenos Aires