Clinical Trials Coordinator & Document Control

Visa Hunt; Argentina; Presencial; ARS 63.416.000 - 96.634.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team. You will ensure timely, accurate task execution across assigned projects within Project Delivery services.

Responsibilities include access management for the project team, document version control, and aiding shipment of trial documentation such as the Investigator Site File. Strong English skills and attention to detail are required.

Formación

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

Responsabilidades

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.).
• Maintain and quality audit to ensure the most recent revisions of documents are on the project portals.
• Assist the project team with the preparation and shipment of clinical trial documentation, including the Investigator Site File.
• Maintain version and quality control of project documentation and submit to the trial master file.
• Assist with the tracking and maintenance of project-related information, including site medical questions and answer logs.

Conocimientos

English proficiency

Educación

Bachelor's degree or equivalent

Herramientas

MS Office

Descripción del empleo

Worldwide Clinical Trials is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team. You will ensure timely, accurate task execution across assigned projects within Project Delivery services.

Responsibilities include access management for the project team, document version control, and aiding shipment of trial documentation such as the Investigator Site File. Strong English skills and attention to detail are required.