Clinical Study Start-Up Lead

IQVIA; Buenos Aires; Presencial; ARS 1.800.000 - 3.000.000; Jornada completa

Descripción de la vacante

IQVIA seeks a seasoned regul​atory/site-activation lead to direct delivery of activation, maintenance and regulatory activities for studies in Argentina. You'll oversee pre-award activities, budget and resources, ensuring regulatory compliance and successful study initiation.

Work closely with Regulatory & Site Activation teams, study management, and multi-regional programs to deliver the agreed scope and maintain quality throughout the lifecycle of trials.

Formación

• Bachelor's degree in life sciences or related field.
• 7 years’ relevant experience in a scientific or clinical environment; international exposure.
• Strong negotiation and communication skills.
• Excellent interpersonal skills and team player.
• Proven ability to manage multiple projects and deadlines.

Responsabilidades

• Direct and manage site activation, maintenance and regulatory activities for studies, including pre-award activities and budget oversight.
• Collaborate across Regulatory & Site Activation, and ensure timely approvals and study initiation; advise on regulatory strategy.

Conocimientos

Regulatory leadership

Clinical trials

Budget management

Cross-functional collaboration

Negotiation

GCP/ICH knowledge

CTMS experience

Educación

Bachelor's Degree Life sciences or related field

Herramientas

CTMS

Regulatory databases

Descripción del empleo

IQVIA seeks a seasoned regul​atory/site-activation lead to direct delivery of activation, maintenance and regulatory activities for studies in Argentina. You'll oversee pre-award activities, budget and resources, ensuring regulatory compliance and successful study initiation.

Work closely with Regulatory & Site Activation teams, study management, and multi-regional programs to deliver the agreed scope and maintain quality throughout the lifecycle of trials.