Global Project Services Manager — Clinical Trials Leadership

IQVIA Argentina; Buenos Aires; Presencial; ARS 1.200.000 - 1.800.000; Jornada completa

Descripción de la vacante

IQVIA Argentina in Buenos Aires is seeking a Manager, Project Services to lead the Client Delivery Team and drive high-quality project management services.

You will mentor staff, plan work, manage performance, and coordinate with internal departments, vendors, sponsors, and regulators throughout the project lifecycle.

This role requires strong English, experience in clinical trials or central laboratory settings, and the ability to navigate FDA/ICH/EMEA guidelines.

Formación

• Bachelor's degree preferred in Life Sciences or related field.
• Minimum 4 years of experience in clinical trials/ hospital-funded research, project management or laboratory environment.
• Advanced English proficiency; CVs must be submitted in English.

Responsabilidades

• Lead, mentor, and develop staff while overseeing day-to-day activities.
• Plan, assign, direct work; manage performance; guide professional development; provide recognition or corrective action.
• Assess project management talent and implement improvements for high-quality service delivery.
• Coordinate cross-functional collaboration across Project Services, internal departments, vendors, sponsors and stakeholders.
• Monitor performance against contractual commitments and project baselines.

Conocimientos

Staff mentoring

Project management

English proficiency

Cross-functional collaboration

Regulatory knowledge

Educación

Bachelor's degree in Life Sciences or related field

Herramientas

Microsoft Office

Descripción del empleo

IQVIA Argentina in Buenos Aires is seeking a Manager, Project Services to lead the Client Delivery Team and drive high-quality project management services.

You will mentor staff, plan work, manage performance, and coordinate with internal departments, vendors, sponsors, and regulators throughout the project lifecycle.

This role requires strong English, experience in clinical trials or central laboratory settings, and the ability to navigate FDA/ICH/EMEA guidelines.