Remote Clinical Research Assistant – Global Trials

Pavago

Buenos Aires

Remote

ARS 900,000 - 1,200,000

Full time

6 days ago
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Job summary

Pavago is seeking an Assistant Clinical Research Associate to support multiple trials and sites. You will assist with remote monitoring, site readiness, and document handling, collaborating with the CRA and Clinical Lead to ensure regulatory compliance.

Responsibilities include training on study systems, coordinating logistics, and maintaining essential documents. A life science degree or RN certification and 0–2 years of related experience are required.

Qualifications

  • Bachelor’s degree in life science or RN certification or equivalent.
  • 0–2 years of relevant experience or equivalent.
  • Familiarity with ICH GCP and regulatory guidelines.

Responsibilities

  • Perform remote monitoring and site support for assigned trials.
  • Assist with site preparedness, EMR/EHR checks, and document collection.
  • Support site management and vendor qualification processes.
  • Coordinate with CRA and Clinical Lead on study activities.
  • Ensure system access and training for site staff.
  • Assist with payments, invoicing, and essential document updates.
  • Maintain study documents and perform reconciliation tasks.
  • Support pre-activation and post-activation activities as directed.

Skills

Medical knowledge
ICH GCP knowledge
Communication skills
Interpersonal skills
Organizational skills
Multitasking
Flexibility
Teamwork
Critical thinking
MS Office proficiency
Information extraction
English proficiency

Education

Bachelor's degree in life science or RN

Job description

Pavago is seeking an Assistant Clinical Research Associate to support multiple trials and sites. You will assist with remote monitoring, site readiness, and document handling, collaborating with the CRA and Clinical Lead to ensure regulatory compliance.

Responsibilities include training on study systems, coordinating logistics, and maintaining essential documents. A life science degree or RN certification and 0–2 years of related experience are required.

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