Parexel

Senior Clinical Research Associate – FSP

Parexel

full-time

Posted on:

Location Type: Remote

Location: Australia

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Job Level

Senior

Tech Stack

Google Cloud Platform

About the role

  • Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP)
  • Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites
  • Serve as the primary point of contact for assigned investigator sites
  • Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities

Requirements

  • Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
  • Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
  • Must be fluent in English and in the native language(s) of the country they will work in
Benefits
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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical trial methodologiessite monitoringstudy monitoring plan (SMP)oncology
Soft Skills
communicationinterpersonal skills
Certifications
ICH/GCP certification