Global Site Activation & Country Approval Specialist

ThermoFisher Scientific; México; Híbrido; MXN 500.000 - 700.000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific is seeking a Site Activation & Country Approval Specialist to support start-up of clinical trials and ensure regulatory compliance. You will collaborate with sites, regulators, sponsors, and internal teams to drive efficient activation and approvals while adhering to SOPs and project timelines.

The role emphasizes regulatory submissions, site activation strategies, and strong quality control across global programs.

Formación

• Bachelor’s degree in Life Sciences or related field, or equivalent experience.
• Strong understanding of clinical research processes and site start-up activities.

Responsabilidades

• Coordinate and support site activation to meet study start-up timelines.
• Prepare and manage regulatory submissions to local authorities and ethics committees.
• Support development of country-specific regulatory strategies.
• Maintain essential site and regulatory documentation per local rules.
• Assist with site agreements, budgets, and document collection.
• Collaborate with investigators, sponsors and internal teams to enable activation.

Conocimientos

Life Sciences

Regulatory Affairs

Clinical operations

Project coordination

Communication

English proficiency

Educación

Bachelor's degree (Life Sciences)

Herramientas

CTMS

Microsoft Office

Descripción del empleo

Thermo Fisher Scientific is seeking a Site Activation & Country Approval Specialist to support start-up of clinical trials and ensure regulatory compliance. You will collaborate with sites, regulators, sponsors, and internal teams to drive efficient activation and approvals while adhering to SOPs and project timelines.

The role emphasizes regulatory submissions, site activation strategies, and strong quality control across global programs.