The opportunity

An exciting opportunity has become available for a part-time Clinical Trial Coordinator to join the team at AR Houston Medical in Kippa-Ring, Queensland. In this role, you will be responsible for coordinating and managing all aspects of clinical trials, ensuring adherence to protocols and regulatory requirements.

Key responsibilities

Coordinate the day-to-day operations of multiple clinical trials, including patient recruitment, scheduling, and data collection

Liaise with study sponsors, principal investigators, and other stakeholders to ensure smooth trial implementation

Monitor study progress and participant safety, and report any issues or concerns to the appropriate parties

Maintain comprehensive and accurate trial records, including case report forms and regulatory documents

Assist with the preparation of study-related materials, such as protocols, informed consent forms, and investigator brochures

Ensure compliance with Good Clinical Practice (GCP) guidelines and all applicable regulations

What we're looking for

Preferred minimum of 2 years' experience as a Clinical Trial Coordinator or in a similar role, but not essential

Strong understanding of clinical research processes, regulations, and Good Clinical Practice guidelines

Excellent organizational and time-management skills, with the ability to prioritize tasks and meet deadlines

Proficient in the use of clinical trial management software and electronic data capture systems

Effective communication and interpersonal skills, with study investigators, sponsors and regulatory bodies

A background in nursing, or research, preferred current APHRA registration

What we offer

At AR Houston Medical, we are committed to providing a supportive and flexible work environment. We offer a competitive salary, opportunities for professional development. If you are passionate about clinical research and are looking to join a dynamic and innovative team, we encourage you to apply now.