Clinical Lab Network Lead - Trials & Customer Liaison

IQVIA Argentina; Santiago; Presencial; CLP 18.000.000 - 36.000.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Descripción de la vacante

IQVIA is seeking a professional to manage laboratory aspects of assigned clinical trial projects for a Customer or program, serving as main contact through the full study lifecycle. Responsibilities include study setup, planning, monitoring, and maintaining documentation in eTMF, while ensuring adherence to SOPs and best practices.

The role requires 2–3 years in clinical trials or related lab environments, strong interpersonal skills, and proficiency with MS Office.

Formación

• Bachelor's degree in life sciences or related field preferred.
• 2–3 years of experience in clinical trials, hospital-funded research, project management, or lab environment.
• Strong interpersonal and customer management skills.
• English language proficiency; local language helpful in some regions.

Responsabilidades

• Manage laboratory aspects of assigned clinical trial projects for a customer or program.
• Serve as main contact for the customer after award and throughout the study lifecycle.
• Lead study setup, planning, timelines, and budget reviews; prepare protocol materials.
• Monitor study activities, documentation, and deviations; coordinate meetings.
• Build and maintain customer relationships and coordinate cross-functional teams.
• Represent the company at investigator meetings and participate in audits.

Conocimientos

Interpersonal skills

Customer management

Communication (English)

Microsoft Office

Educación

Bachelor's Degree Life Sciences or related field

Herramientas

Microsoft Office

Descripción del empleo

IQVIA is seeking a professional to manage laboratory aspects of assigned clinical trial projects for a Customer or program, serving as main contact through the full study lifecycle. Responsibilities include study setup, planning, monitoring, and maintaining documentation in eTMF, while ensuring adherence to SOPs and best practices.

The role requires 2–3 years in clinical trials or related lab environments, strong interpersonal skills, and proficiency with MS Office.