Remote Clinical Project Manager – Study Delivery & Compliance

Caylent, Inc.; Partido de Quilmes; A distancia; ARS 1.200.000 - 1.800.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible work schedule

Home-based position

Ongoing learning and development

Descripción de la vacante

Indero is seeking a Project Manager to ensure initiation, planning, execution, monitoring and closure of clinical research projects in Argentina. You will ensure adherence to the study budget, scope and timelines, under supervision by senior PM/Program Director.

The role emphasizes GCP, SOPs and regulatory compliance. The ideal candidate has experience in clinical studies, strong PM discipline, and a drive to advance to project management leadership, with a home-based/remote setup available in

Formación

• B.Sc. in a related field required.
• 3+ years managing clinical studies in pharma/biotech/CRO.
• 2+ years coordinating clinical trial management.
• Excellent knowledge of GCP/ICH; FDA/Canadian regs advantageous.
• English proficiency required; French is a plus.

Responsabilidades

• May serve as primary contact for Sponsor, vendors and internal team.
• Coordinate tasks and deadlines between departments.
• Oversee project coordinators and resources to prioritize site activation.
• Coordinate vendor supplies and services with site activation timelines.
• Escalate at risk timelines to PM II.
• Assist with sponsor needs and stakeholder expectations.
• Ensure team training on the project.
• Develop and manage project activities and resources.

Conocimientos

GCP/ICH standards

Microsoft Office

English proficiency

Team collaboration

Problem solving

Project management discipline

Organizational skills

Educación

B.Sc. in a related field

Herramientas

Microsoft Office

Descripción del empleo

Indero is seeking a Project Manager to ensure initiation, planning, execution, monitoring and closure of clinical research projects in Argentina. You will ensure adherence to the study budget, scope and timelines, under supervision by senior PM/Program Director.

The role emphasizes GCP, SOPs and regulatory compliance. The ideal candidate has experience in clinical studies, strong PM discipline, and a drive to advance to project management leadership, with a home-based/remote setup available in