Remote Clinical Trials Associate: Study Coordination

Worldwide Clinical Trials Co., Ltd.; Argentina; A distancia; ARS 78.757.000 - 93.902.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Clinical Trials Associate for a remote role available to candidates based in Argentina, Mexico, or Brazil. You will provide administrative and project-tracking support to clinical project teams, facilitating timely documentation, system access, and training coordination to keep studies inspection-ready.

You will work with Project Managers and CRAs to ensure quality and compliant study delivery.

Formación

• Degree-level qualification or equivalent experience, plus a minimum of one year of experience in a related role.

Responsabilidades

• Coordinate and track system access for project team members, including Project Managers, Lead CRAs, and CRAs.
• Maintain project portals and perform quality checks to ensure teams have access to the most current versions of documents.
• Support the preparation, shipment, version control, and filing of clinical trial documentation, including Investigator Site Files and Trial Master File documentation.
• Track and maintain project information, including site medical question and answer logs and participating site and personnel details.
• Prepare and distribute accurate meeting minutes for sponsor, project, and internal management meetings.
• Coordinate and track project-specific training to help ensure project teams remain up to date with required information.

Conocimientos

English proficiency

Organizational skills

Attention to detail

Microsoft Office

Educación

Bachelor's degree or equivalent

Descripción del empleo

Worldwide Clinical Trials is seeking a Clinical Trials Associate for a remote role available to candidates based in Argentina, Mexico, or Brazil. You will provide administrative and project-tracking support to clinical project teams, facilitating timely documentation, system access, and training coordination to keep studies inspection-ready.

You will work with Project Managers and CRAs to ensure quality and compliant study delivery.