Clinical Trials Site Activation Coordinator

Virtustant; Buenos Aires; Remote; ARS 84,554,000 - 115,301,000; Full time

Job summary

Virtustant in the Buenos Aires area seeks a Clinical Trial Coordinator II to support site activation and trial documentation under supervision. You will work with the Project Team to ensure regulatory and study requirements are met, maintaining timelines and quality standards.

You will review files, assist with regulatory submissions, ISF maintenance, and coordinate with sites and internal teams to keep studies on track.

Qualifications

• Bachelor's degree in Life Sciences or a related field.
• At least 1 year of clinical research experience.
• Advanced level of English – you’ll be working with North American sites.

Responsibilities

• Coordinate, oversee and complete functions on assigned trial activities.
• Review Internal, Country and Investigator file reviews and document findings.
• Ensure tasks are performed on time, within budget and to high quality standards.
• Process documents for Client (eTMF), perform reviews and distribute communications.
• Maintain site regulatory documents and ISF/Pharmacy binder materials as needed.
• Support start-up activities, regulatory submissions and site activation timelines.

Skills

Clinical research

English proficiency

Education

Bachelor's degree Life sciences or related field

Job description

Virtustant in the Buenos Aires area seeks a Clinical Trial Coordinator II to support site activation and trial documentation under supervision. You will work with the Project Team to ensure regulatory and study requirements are met, maintaining timelines and quality standards.

You will review files, assist with regulatory submissions, ISF maintenance, and coordinate with sites and internal teams to keep studies on track.