Senior Clinical Trial Manager, Ambulatory Trials

Clinica Nueva Esperanza

Santiago

Presencial

CLP 58.027.000 - 87.041.000

Jornada completa

Hace 9 días
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Descripción de la vacante

Thermo Fisher Scientific in Santiago is seeking a Senior Clinical Trial Manager to lead trials, ensure data integrity, and manage timelines across regional projects. The role emphasizes achieving contractual deliverables with quality, cost control, and profitability while coordinating with cross-functional teams.

The Senior CTM will oversee monitoring plans, CRFs, and regulatory interactions, driving process improvements and ensuring compliance with ICH/GCP and FDA guidelines.

Formación

  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
  • 8+ years of experience in a similar role or higher.
  • Equivalency may be considered with related education, training or experience.

Responsabilidades

  • Manage all clinical operational and quality aspects of allocated studies in compliance with ICH GCP.
  • Develop clinical tools and the MAP; ensure timely set up and quality of Trial Master File.
  • Collaborate with project manager for client meetings and bid defenses.
  • Implement standardized monitoring processes; ensure timely archiving of documents.
  • Provide input into forecast estimates and manage clinical resources and budgets.

Conocimientos

Leadership
Planning
Interpersonal skills
Change management
Clinical monitoring
Budgeting
English proficiency
Communication
Prioritization

Educación

Bachelor's degree or equivalent

Herramientas

Outlook
Excel
Word

Descripción del empleo

Thermo Fisher Scientific in Santiago is seeking a Senior Clinical Trial Manager to lead trials, ensure data integrity, and manage timelines across regional projects. The role emphasizes achieving contractual deliverables with quality, cost control, and profitability while coordinating with cross-functional teams.

The Senior CTM will oversee monitoring plans, CRFs, and regulatory interactions, driving process improvements and ensuring compliance with ICH/GCP and FDA guidelines.

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