Country Trial Lead: Complex Studies & Site Optimization

IQVIA Argentina; Boston (MA); On-site; USD 93,000 - 233,000; Full time

Job summary

IQVIA is seeking a driven trial manager to lead country-level execution for complex clinical studies in the US. The role requires managing timelines, budgets, and regulatory readiness, while coordinating with sponsors and CRO partners to ensure high-quality data and patient safety.

You will contribute to site management, CAPA implementation, and inspection readiness, with travel as needed to investigator meetings and sites across regions.

Qualifications

• 3 to 5+ years of trial management experience.
• Strong working knowledge of ICH-GCP, Sponsor SOPs, local regulations.
• Willingness to travel as required by business needs.
• Proficient in English, strong written and oral communication.

Responsibilities

• Lead country-level trial management activities for complex studies.
• Coordinate with cross-functional teams and external partners.
• Monitor study progress, timelines, and budget; report risks and CAPAs.
• Ensure regulatory approvals and trial documentation are compliant.
• Manage site performance, data quality, and patient safety oversight.

Skills

Trial management

ICH-GCP knowledge

Sponsor SOPs

English proficiency

Travel willingness

Education

BA/BS degree

Health/science field degree

Tools

CTMS

Job description

IQVIA is seeking a driven trial manager to lead country-level execution for complex clinical studies in the US. The role requires managing timelines, budgets, and regulatory readiness, while coordinating with sponsors and CRO partners to ensure high-quality data and patient safety.

You will contribute to site management, CAPA implementation, and inspection readiness, with travel as needed to investigator meetings and sites across regions.