Clinical Trials Coordinator

3 days ago

Melbourne, Victoria, Australia beBeeClinicalResearchAssociate Full time
Job Overview

We are seeking a highly motivated and detail-oriented Clinical Research Associate I to support the planning, execution, and monitoring of clinical trials. This role is ideal for individuals with a strong passion for healthcare and a desire to work in a fast-paced environment.

The Clinical Research Associate I will be responsible for supporting site selection, initiation, and monitoring visits, as well as reviewing study documentation and data for accuracy and completeness. This role requires excellent organizational skills, attention to detail, effective communication, and a foundational understanding of Good Clinical Practice (GCP) and relevant regulations.

Main Responsibilities:

  • Support site selection, initiation, and monitoring visits
  • Review study documentation and data for accuracy and completeness
  • Liaise with site staff to address study-related issues
  • Evaluate and ensure effective recruitment and retention techniques based on the patient disease journey
  • Develop fundamental knowledge connecting the study protocol, scientific principles, and clinical trial requirements to day-to-day trial activities
  • Monitor activities conducted by clinical sites to detect early study performance or patient safety issues
  • Implement preventative and corrective actions to mitigate risks and promote compliance using a customer-centric approach
  • Ensure data quality from study sites and timely submission of data, including safety reporting

Required Skills and Qualifications:

  • Tertiary qualification in a health-related discipline (Medical, Scientific, Nursing)
  • Knowledge of therapeutic area indications, with the ability to understand and apply scientific concepts related to clinical trials
  • Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies
  • Experience in clinical research coordination or data management preferred
  • Ability to work collaboratively across functions to develop and maintain relationships
  • Strong planning and organizational skills to work effectively in a dynamic environment with multiple deadlines
  • Proficiency in leveraging technology and tools to support site health and clinical trial activities
  • Strong interpersonal, communication, and presentation skills to establish trusted site relationships

Benefits:

This is a unique opportunity to work with a reputable organization recognized for its commitment to innovation, community service, diversity, and inclusion. As an employee, you will have access to professional development opportunities, flexible working arrangements, and a comprehensive benefits package.

Other Opportunities:

This role offers a challenging and rewarding experience that will allow you to grow your skills and expertise while making a meaningful contribution to the success of our organization. If you are a motivated and results-driven individual looking for a new challenge, we encourage you to apply for this exciting opportunity.

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