Lab Project Coordinator - Accelerate Clinical Trials

IQVIA LLC; Buenos Aires; Híbrido; ARS 1.200.000 - 1.800.000; Jornada completa

Descripción de la vacante

IQVIA LLC in Buenos Aires seeks a Laboratory Project Services Coordinator to manage laboratory-related aspects of clinical trial projects from startup through closeout. You will partner with the Project Manager and cross-functional teams to keep work on track, communicate progress, and ensure high-quality execution across studies.

The role requires a Bachelor’s degree and experience coordinating clinical trial or laboratory operations, with strong English and proficiency in MS Office.

Formación

• Bachelor’s degree in any discipline is required.
• Experience supporting clinical trial or laboratory operations projects is preferred.
• Proficiency with project tracking and documentation tools and strong English skills.

Responsabilidades

• Support the Project Manager with study initiation activities, including required documentation, coordination, and readiness tracking.
• Coordinate day-to-day laboratory project activities to support delivery of timelines and client expectations.
• Serve as a key point of contact for assigned clients after study award, maintaining clear and timely communications.
• Monitor project status, identify risks or blockers, and escalate with proposed mitigation actions.
• Manage multiple priorities across mid-size and large pharma accounts, balancing urgency and accuracy under pressure.
• Leverage internal team members and stakeholders to resolve issues and keep deliverables moving.

Conocimientos

Highly organized

Attention to detail

Excellent communication

Project coordination

Educación

Bachelor's degree in any discipline

Herramientas

MS Office/Excel

Project trackers

Descripción del empleo

IQVIA LLC in Buenos Aires seeks a Laboratory Project Services Coordinator to manage laboratory-related aspects of clinical trial projects from startup through closeout. You will partner with the Project Manager and cross-functional teams to keep work on track, communicate progress, and ensure high-quality execution across studies.

The role requires a Bachelor’s degree and experience coordinating clinical trial or laboratory operations, with strong English and proficiency in MS Office.