Laboratory Network Lead - Clinical Trials & Management

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

Descripción de la vacante

IQVIA is recruiting to manage all laboratory aspects for assigned clinical trial projects and serve as the main contact with customers throughout the study lifecycle. You will ensure adherence to SOPs and support study startup, maintenance, and closeout activities.

The role requires 2–3 years of clinical trials or laboratory project management experience, strong interpersonal and communication skills, and proficiency in MS Office.

Formación

• Bachelor's degree in Life Sciences or related field.
• 2–3 years in clinical trials, project management, or lab environment.
• Strong interpersonal and customer management skills.
• Familiarity with clinical research terminology and PM processes.
• Experience with central laboratory operations is a plus.
• Proficient in MS Office and company systems.
• Experience leading Phase I–IV trials.
• Able to work in fast-paced environments and meet deadlines.
• Strong written and verbal English; local language knowledge is a plus.

Responsabilidades

• Manage laboratory aspects of assigned clinical trial projects and serve as primary customer contact.
• Oversee study setup, protocol documentation, and budget reviews.
• Monitor project plans, timelines, deliverables, and study documentation.
• Coordinate communications across operational areas and triage issues.
• Represent the company at meetings and support audits/inspections.
• Provide training to sites, CRAs, and customers.

Conocimientos

Interpersonal skills

Customer management

Communication skills

English language proficiency

Project management

Organizational skills

MS Office

Educación

Bachelor's Degree Life Sciences

Herramientas

Microsoft Office

Descripción del empleo

IQVIA is recruiting to manage all laboratory aspects for assigned clinical trial projects and serve as the main contact with customers throughout the study lifecycle. You will ensure adherence to SOPs and support study startup, maintenance, and closeout activities.

The role requires 2–3 years of clinical trials or laboratory project management experience, strong interpersonal and communication skills, and proficiency in MS Office.