Remote Assistant Clinical Research Associate

Afnord Pmo

Quilmes

Hybrid

ARS 55,635,000 - 92,724,000

Full time

4 days ago
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Job summary

Thermo Fisher Scientific is seeking an Assistant Clinical Research Associate to support site readiness, monitoring logistics, and remote study management in accordance with SOPs and regulatory guidelines. You may assist with limited site contact during start-up, site management, recruitment and close-out phases.

Responsibilities include coordinating training, reviewing study materials, ensuring system access, and supporting vendor qualification and payments across trials with occasional travel.

Qualifications

  • Knowledge of ICH GCP, applicable regulations and SOPs.
  • Strong medical terminology and clinical trial literacy.
  • Excellent written and verbal communication in English.

Responsibilities

  • Assist with study and site management activities as defined for the assigned trial.
  • Complete and document study-specific training and system orientation.
  • Support pre-study assessments and site coordination activities as required.
  • Assist in customizing Site ICF with site details.
  • Support remote review of EMR/EHR checklists and data collection.
  • Verify document collection and trial tracking statuses.
  • Contribute to vendor qualification and system access processes.
  • Coordinate with site staff and other departments on logistics and payments.

Skills

ICH GCP
Medical terminology
Communication skills
MS Office
English language

Education

Bachelor's degree in life science
Registered Nursing certification

Tools

CTMS
EHR systems
Dashboards

Job description

Thermo Fisher Scientific is seeking an Assistant Clinical Research Associate to support site readiness, monitoring logistics, and remote study management in accordance with SOPs and regulatory guidelines. You may assist with limited site contact during start-up, site management, recruitment and close-out phases.

Responsibilities include coordinating training, reviewing study materials, ensuring system access, and supporting vendor qualification and payments across trials with occasional travel.

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