Clinical Research Associate

3 weeks ago

Sydney, New South Wales, Australia BeiGene Full time

Clinical Research Associate Role Overview:

The Clinical Research Associate (CRA) is responsible for monitoring clinical trials in Oncology and Hematology within the country. This involves ensuring that data is collected and delivered within timelines and quality standards, adhering to GCP, ICH, local regulations, and SOPs.

Key Responsibilities:

  • Conduct monitoring visits, co-monitoring visits, and quality oversight visits as required.
  • Ensure study milestones are met, including study startup, recruitment, database analysis, and closeout.
  • Qualification and Skills:
    • Bachelor's degree in life sciences, pharmacy, nursing, or medicine.
    • 1+ year of monitoring experience in the pharmaceutical or CRO industry.
    • Excellent communication, interpersonal, and organizational skills.
    • Fluent in English (writing and speaking).
    • Full Australian working rights required.

    What We Offer:

    • Market competitive compensation package with annual bonus scheme.
    • Company shares with welcome grant and performance-based equity plan.
    • Learning and development opportunities.
    • Fantastic benefits program.
    • Dynamic team environment.
    • Opportunity to work with a global company dedicated to cancer treatment.

    BieiGene Global Competencies:

    • Fostering teamwork and collaboration.
    • Providing honest and actionable feedback.
    • Self-awareness and adaptability.
    • Acting inclusively and respectfully.
    • Demonstrating initiative and entrepreneurial spirit.
    • Embracing change and driving excellence.
    • Results-oriented and analytical thinking.
    • Communicating effectively and clearly.

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