Field Clinical Trial Lead - Site Coordination

Iqvia; Ciudad de Mendoza; On-site; ARS 43,046,000 - 73,793,000; Full time

Job summary

Iqvia is seeking a Milestone One Site Coordinator to support trial sites in all related activities in line with ICH-GCP and study timelines. You will act as the primary liaison between sponsors/CROs and the site, manage feasibility responses, schedule monitoring visits, and ensure accurate data handling and documentation across sites.

The role requires at least 3 years in a clinical trial setting, strong English, and the ability to work in a fast-paced, global team environment.

Qualifications

• College or university degree in Life Science, preferably in pharmacy, nursing or lab analytics.
• Minimum of 3 years of on-the-job experience in a clinical trial environment, as Study Coordinator or similar.
• Upper-Intermediate English, able to work in a global team.

Responsibilities

• Act as the main line of communication between the Sponsor or CRO and the site.
• Ensure response to feasibility questions in due time.
• Assist in scheduling and preparation for monitoring visits.
• Be present and available to respond to monitors during visits conducted at the medical institution.
• Track patient enrollment and support timelines and enrollment goals.
• Maintain study documents at the site level.
• Accurate data entry into EDC systems and timely resolution of data clarification queries.
• Timely reporting and follow up on Adverse Events and Protocol Deviations.
• Proper handling, accountability and reconciliation of investigational products and clinical supplies.
• Collect, handle and maintain site regulatory documents as needed.
• Facilitate and support contract and budget negotiations at the site level.
• Support Investigator and Site payments and processes as needed.
• Schedule and/or perform study procedures and delegation of responsibilities.
• Prepare for and participate in onsite study audits or regulatory agency inspections.
• Build and sustain relationships with sponsors, CROs, and medical institutions.

Skills

Communication

English proficiency

Time management

Problem solving

Education

Life Science degree

Job description

Iqvia is seeking a Milestone One Site Coordinator to support trial sites in all related activities in line with ICH-GCP and study timelines. You will act as the primary liaison between sponsors/CROs and the site, manage feasibility responses, schedule monitoring visits, and ensure accurate data handling and documentation across sites.

The role requires at least 3 years in a clinical trial setting, strong English, and the ability to work in a fast-paced, global team environment.