Senior Clinical Trial Monitor

1 week ago

Armidale, New South Wales, Australia beBeeClinical Full time $80,000 - $100,000

Job Summary:

We are seeking a skilled Clinical Trial Monitoring professional to join our team.

About the Role:

  • Lead the monitoring of clinical trials, ensuring adherence to Study Monitoring Plans and relevant regulations.
  • Manage operational aspects, including site activation, data collection, and quality assurance.

Main Responsibilities:

  • Serve as primary point of contact for investigator sites, providing support and guidance as needed.
  • Collaborate with the Study Coordinating Partner (SCP) to ensure high-quality site delivery.
  • Facilitate communication between study team members, vendors, and investigator sites.

Requirements:

  • Bachelor's degree in life sciences or a related field.
  • Strong knowledge of clinical trial methodologies, ICH/GCP, FDA, and local regulations.
  • At least 2 years of experience in clinical research site monitoring and management.

What We Offer:

  • A competitive salary package.
  • An inclusive and accessible work environment.

About Our Company:

Inclusion and belonging are fundamental to our culture and values. We strive to create an environment where everyone can thrive.

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