Global Clinical Trial Site Lead

Visit.Org, Inc.

Ciudad de Mendoza

Remote

ARS 45,437,000 - 69,670,000

Full time

4 days ago
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Job summary

Visit.Org, Inc. is seeking a Milestone One Site Coordinator to support trial sites in accordance with ICH-GCP, ensuring adherence to protocol requirements and timelines.

You will act as the primary liaison between sponsors, CROs, and sites, coordinating monitoring visits and maintaining regulatory documents. The role requires a Life Science degree with at least 3 years in a clinical trial setting, plus an upper-intermediate level of English to operate within a global team and handle fast-paced,

Qualifications

  • Degree in Life Science or related field.
  • Minimum 3 years in a clinical trial environment as a Study Coordinator or similar.
  • Upper-Intermediate level of English to work in a global team.
  • Ability to manage multiple tasks with short timelines.
  • Strong communication and problem-solving abilities.

Responsibilities

  • Act as the main line of communication between the Sponsor or CRO and the site.
  • Ensure timely response to feasibility questions.
  • Assist in scheduling and preparation for all monitoring visits at the site.
  • Be present and available to respond to monitors during visits.
  • Track patient enrollment and support timelines and enrollment goals.
  • Maintain study documents at the site level and ensure data entry accuracy.
  • Support regulatory documents handling and site-related inspections.

Skills

English (Upper-Intermediate)
Communication
Time management
Team collaboration

Education

Life Science degree (pharmacy/nursing/lab analytics)

Job description

Visit.Org, Inc. is seeking a Milestone One Site Coordinator to support trial sites in accordance with ICH-GCP, ensuring adherence to protocol requirements and timelines.

You will act as the primary liaison between sponsors, CROs, and sites, coordinating monitoring visits and maintaining regulatory documents. The role requires a Life Science degree with at least 3 years in a clinical trial setting, plus an upper-intermediate level of English to operate within a global team and handle fast-paced,

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