Clinical Trial Coordinator: Site Activation & Compliance

ThermoFisher Scientific; Argentina; Remote; ARS 90,953,000 - 136,430,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Clinical Trial Coordinator to support project teams across regulatory and site activation activities.

You will provide administrative and system support (eTMF/CTMS), review documents, and help develop the site activation plan while ensuring compliance with SOPs and sponsor directives. Strong English and local language skills, plus MS Office proficiency, are required.

Qualifications

• High/secondary diploma or equivalent; Bachelor's degree preferred.
• Experience related to clinical trial coordination (0–1 year).
• Strong English and local language skills; proficient in MS Office.

Responsibilities

• Coordinate and complete trial activities as detailed in the task matrix.
• Review and document findings in appropriate systems.
• Ensure tasks are on time and within budget; escalate risks.
• Provide system support for Activate and eTMF; keep databases current.
• Assist with site activation documents and regulatory submissions.

Skills

Teamwork

Organizational skills

Attention to detail

Data analysis

Customer focus

Flexibility

Regulatory knowledge

English proficiency

MS Office

Communication

Education

Bachelor's degree preferred

High/Secondary diploma or equivalent

Tools

CTMS

eTMF

MS Office

Job description

Thermo Fisher Scientific is seeking a Clinical Trial Coordinator to support project teams across regulatory and site activation activities.

You will provide administrative and system support (eTMF/CTMS), review documents, and help develop the site activation plan while ensuring compliance with SOPs and sponsor directives. Strong English and local language skills, plus MS Office proficiency, are required.