Clinical Trial Specialist

3 days ago

Sydney, New South Wales, Australia beBeeResearch Full time $80,000 - $90,000

Clinical Research Associate I Role

The primary responsibility of this role is to support the planning, execution, and monitoring of clinical trials. This includes ensuring compliance with regulatory guidelines, protocols, and quality standards.

Key Responsibilities:

  • Act as the primary point of contact for investigative sites, providing contextual information on clinical trials and strengthening positioning.
  • Align, train, and motivate site staff and principal investigators on the goals of clinical trial programs, protocol, and patient treatment principles.
  • Conduct site evaluation, site training, routine, and site closure monitoring activities under supervision, in compliance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, and Standard Operating Procedures (SOPs).

Requirements:

  • Tertiary qualification in a health-related discipline such as medical, scientific, or nursing.
  • Knowledge of appropriate therapeutic area indications and ability to understand and apply scientific concepts as they relate to the conduct of clinical trials.
  • Clinically related experience preferably in clinical research coordinating or data management.

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