Trial Research Associate

2 weeks ago

Sydney, New South Wales, Australia beBeeClinicalResearch Full time $113,000 - $123,000
Job Overview

The UNSW Trial Coordinator role is a critical component of the Parent-Child Research Clinic (PCRC) in the School of Psychology. This prestigious clinic conducts cutting-edge research at the intersection of developmental and clinical psychology to advance early intervention for childhood mental disorders.

Key Responsibilities
  • Develop and refine study materials in line with International Council for Harmonisation Guidelines and regulatory standards.
  • Coordinate project meetings and oversee externally funded projects to meet trial protocols and milestones.
  • Effectively manage recruitment, screening, scheduling, tracking, and follow-up procedures for participants in multi-site clinical research trials.
  • Maintain efficient systems for scheduling, communication, file organisation, and documentation of meetings and study procedures.
  • Perform tasks associated with undertaking research trials, including scoring measures, literature reviews, data collection, entry, management, analysis, and administrative duties.
  • Monitor adverse events and ensure proper documentation and reporting.
  • Nurture effective working relationships with stakeholders and coordinate with governmental departments, media outlets, and school stakeholders.
  • Travel to trial sites for training, on-site monitoring, and coordination duties.
  • Identify funding opportunities and prepare grant applications.
  • Act as the first point of contact for internal and external stakeholders, maintaining channels of communication and analysing requests and correspondence.
  • Manage invoicing and financial processing for clinic activities.
  • Assist with report preparation and submission based on research conducted.
Required Skills and Qualifications
  • A postgraduate qualification or equivalent knowledge gained through education, training, or experience.
  • Demonstrated clinical trial coordination experience, including protocol development, data management systems, governance, monitoring, and reporting.
  • Excellent organisational skills, written, verbal, and interpersonal skills, and ability to communicate effectively with stakeholders.
  • Demonstrated experience providing administrative and research support, with attention to detail and accuracy.
  • Experience with research data management and statistical analysis using statistical software.
  • Demonstrated knowledge of HREC and regulatory applications, such as GCP and reporting for clinical trials.
  • Skills in project management, statistical software packages, and statistical analysis.
  • Ability to implement required health and safety policies and procedures.
Benefits
  • This is a full-time, fixed-term position for 2 years at a salary range plus Superannuation and annual leave loading.
About The Successful ApplicantSelection Criteria
  • A strong academic background and relevant industry experience.
  • Demonstrated ability to work collaboratively in a team environment.
  • Excellent time management and organisational skills.

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