Are you an expert in your field of medicine and interested to contribute to clinical trial outcomes but wonder how to integrate a clinical trial into your practice?

Engage a Dedicated Clinical Trial Coordinator to manage the overlapping clinical, administrative, regulatory and budgetary tasks on a contract basis.

• A Dedicated CRC is a Nurse registered with AHPRA and is ICHGCP certified.

• A Dedicated CRC will coordinate clinical trial functions with minimal disruption to the wider practice on a contract basis.

• A dedicated CRC has strong clinical background

• Dedicated to the protection of those who participate in a clinical trial

• Trained by the Sponsor in all aspects of the study and is supported by a backup CRC who is equally trained.

• A coordinator of administrative and clinical aspects of the study and the quality of the data generated.

• Highly organised and people orientated.

• A problem solver seeking to deliver solutions to challenges at site level.

• Committed to high standards in all areas of study conduct.

• An insightful and cooperative professional who is a team player.

• A good listener who shows empathy for others.

• Respectful of the needs of the patient

• Flexible, attending site only as needed and otherwise works remotely.

• A focused, critical thinker who maintains the safety and wellbeing of participants as the highest priority.

• Understands the importance of clinical research as the pathway for new treatments for all and is dedicated to achieving the objectives.

• An energetic multitasker whose friendliness and cooperation makes them a pleasure to be around.