Global Clinical Trial Lead - End-to-End Program Manager

IQVIA Argentina; Buenos Aires; Híbrido; ARS 900.000 - 1.500.000; Jornada completa

Descripción de la vacante

IQVIA Argentina is seeking a Senior Clinical Project Manager to oversee global clinical trial management from start-up to closeout. You will ensure delivery in line with ICH/GCP, protocol, and contract requirements while leading recruitment and risk mitigation efforts.

The role requires a strong background in GCP/ICH, extensive trial management experience, and budgeting capabilities. A favorable candidate will have knowledge of local regulations and a track record in multi-site/global trials.

Formación

• Bachelor’s degree in health care or another scientific discipline is required.
• 8 years of clinical research/monitoring experience or equivalent.
• Min 3 years of regional/global trial management experience in pharma or CRO.
• In-depth knowledge of GCP and ICH guidelines.

Responsabilidades

• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (GCP, ICH), protocol, contracts, and SOPs.
• Be accountable for meeting recruitment targets and implementing recruitment strategies.
• Contribute to risk mitigation planning and manage clinical risks across the project lifecycle.
• Ensure clinical quality delivery by identifying and measuring quality standards and addressing issues.

Conocimientos

GCP & ICH knowledge

Clinical trial management

Budget & finances

Regulatory compliance

Global trial mgmt

Educación

Bachelor’s degree in Health care or science

Descripción del empleo

IQVIA Argentina is seeking a Senior Clinical Project Manager to oversee global clinical trial management from start-up to closeout. You will ensure delivery in line with ICH/GCP, protocol, and contract requirements while leading recruitment and risk mitigation efforts.

The role requires a strong background in GCP/ICH, extensive trial management experience, and budgeting capabilities. A favorable candidate will have knowledge of local regulations and a track record in multi-site/global trials.