U

University of Sydney

Genetics Research Coordinator

Medical ResearchPosted on Nov 13
Part-timeCamperdown, Australia

About the Job

Requirements

  • A bachelor's degree in a relevant discipline, or an equivalent combination of training and experience.
  • Demonstrated experience supporting or coordinating clinical trials within a research, health, academic, or public health environment.
  • Knowledge of International Council for Harmonisation (ICH) Guidelines and Good Clinical Practice (GCP) requirements.
  • Experience coordinating ethics submissions, research governance activities, or regulated research programs.
  • Experience maintaining accurate records, managing research data, and producing reports.
  • Strong organisational skills with the ability to manage competing priorities across multiple stakeholders and projects.
  • Excellent written and verbal communication skills, including the ability to engage effectively with researchers, clinicians, schools, community groups, and healthcare stakeholders.
  • Demonstrated attention to detail and commitment to quality, compliance, and ethical research practices.
  • Proficiency using research-related systems, databases, and standard business software applications.
  • Unrestricted work rights in Australia for the duration of employment are required; visa sponsorship is not available.
  • A Working with Children Check clearance is required.

Responsibilities

  • Coordinate the delivery of the research program across collaborating institutions and project work packages.
  • Develop and maintain effective relationships with clinicians, industry and community partners, sponsors, and other key stakeholders.
  • Support end-to-end delivery of research activities, including study start-up, participant coordination, data collection, and close-out activities.
  • Maintain accurate clinical trial documentation and data records in accordance with regulatory, ethical, and Good Clinical Practice (GCP) requirements.
  • Prepare and coordinate ethics and governance submissions, grant reporting requirements, and compliance activities.
  • Coordinate reporting activities, monitor data integrity, and support compliance initiatives across clinical research projects.
  • Manage purchasing, invoicing, and payment processes related to research activities.
  • Contribute to risk management, protocol review activities, and continuous improvement initiatives that support a strong safety culture.
  • Facilitate communication across a broad range of stakeholders to support successful research outcomes and participant engagement.

Desired Qualifications

  • Experience working with schools, community organisations, healthcare providers, or research participants.

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