Sponsor-Dedicated Clinical Trial Manager

IQVIA LLC; Buenos Aires; On-site; ARS 1,200,000 - 1,800,000; Full time

Job summary

IQVIA LLC is seeking a Clinical Trial Manager – Sponsor Dedicated to oversee local trial management from start-up through closeout, ensuring compliance with ICH-GCP, Sponsor SOPs, and regulatory requirements.

You will manage budgets and contracts, monitor timelines and patient recruitment, support inspections and audits, and coordinate with country teams to drive study progress and data integrity.

Qualifications

• BA/BS degree required.
• Degree in health or science field.
• Minimum 2 years local/regional trial management experience.
• Knowledge of ICH-GCP, SOPs and local regulations.
• Strong IT skills in appropriate software and company systems.
• Willingness to travel with occasional overnight stays.
• Excellent decision-making and financial management skills.
• Proficient in speaking and writing English and the country language.

Responsibilities

• Adheres to Sponsor SOPs, WIs, policies, and GCP; complies with local regulatory requirements.
• Contributes to high-level budget estimates and contract management.
• Acts as primary country contact and tracks project progress locally.
• Monitors patient recruitment and enrollments; supports contingency planning.
• Maintains trial management systems, reports, and supports HA inspections and audits.
• Supports site-level recruitment strategy with cross-functional teams.
• Reviews country-specific informed consent in line with SOPs and regulations.

Skills

Trial management

Communication

Decision making

Financial management

Travel willingness

Bilingual English

Education

B.A./B.S. degree

Health or science degree

Job description

IQVIA LLC is seeking a Clinical Trial Manager – Sponsor Dedicated to oversee local trial management from start-up through closeout, ensuring compliance with ICH-GCP, Sponsor SOPs, and regulatory requirements.

You will manage budgets and contracts, monitor timelines and patient recruitment, support inspections and audits, and coordinate with country teams to drive study progress and data integrity.