Clinical Trial Site Activation Coordinator

Virtustant

Quilmes

A distancia

ARS 76.867.000 - 107.614.000

Jornada completa

Hace 13 días

Una candidatura completa en un minuto

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Descripción de la vacante

Virtustant is seeking a Clinical Trial Coordinator II to support site activation activities and regulatory submissions for investigative sites in a dynamic pharmaceutical operations environment. The role requires coordination with the Project Team, completion of regulatory and ethics documents, and timely management of site file reviews and communication with sites.

A bachelor’s degree in life sciences and 1+ year of clinical research experience are preferred, with advanced English required.

Formación

  • Bachelor's Degree Life sciences or a related field.
  • At least 1 year of clinical research experience.
  • Advanced level of English.

Responsabilidades

  • Serve as a Single Point of Contact (SPOC) to perform feasibility and site activation activities with investigative sites.
  • Review documents for completeness and accuracy under guidance of senior staff.
  • Prepare and review site documents, regulatory filings, and ISF/ICF materials.
  • Assist with coordination, tracking, and documentation of regulatory submissions and site start-up activities.
  • Maintain internal tracking tools, timelines, and project plans with accurate information.
  • Support cross-functional teams and ensure site activation tasks are completed on time and within budget.

Conocimientos

English proficiency
Regulatory awareness
Documentation review

Educación

Bachelor's degree Life sciences or related field

Descripción del empleo

Virtustant is seeking a Clinical Trial Coordinator II to support site activation activities and regulatory submissions for investigative sites in a dynamic pharmaceutical operations environment. The role requires coordination with the Project Team, completion of regulatory and ethics documents, and timely management of site file reviews and communication with sites.

A bachelor’s degree in life sciences and 1+ year of clinical research experience are preferred, with advanced English required.

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