• Clinical Trials • Multiple Therapeutic Areas • Opportunity for Expansion! Our client has decades of experience conducting clinical trials in multiple therapeutic areas, providing the best outcomes for participants and sponsors. Their network of sites in Sydney and Melbourne conduct Phase I to Phase IV trials in purpose built out-patient facilities. Working closely with their sponsor’s teams and understanding their sponsor’s objectives allows them to implement a tailored approach to meet their clinical trial requirements. As a Consultant Principal Investigator, you will have the opportunity to get involved in a wide range of studies and have academic opportunities to publish research papers with one of the fastest growing clinical research organisations in Australia. Driven and focused, you are strategically aware, anticipating business and client needs and adapting to meet these needs. You are a natural innovator; action focused and display mature clinical and business judgement. The Role Business Growth:  Promote site capabilities and performance through positive engagement with Sponsors, Clinical Research Organizations, regulatory authorities and other stakeholders  Diplomatic when managing Sponsor queries and concerns, and matters related to staff  Actively engage with the Business Development team  Consult with the OM to optimise recruitment opportunities for all participants.  Build and maintain a close relationship with our recruitment partners  Tailor pre-screening activities as required by the protocol and the business  Implement solutions to challenges that impede recruitment efforts.  Act as a consultant for study feasibility reviews  Attend conferences both local and international Business Efficiency:  Key resource person for the Trial Advancement Team (TAT) – close collaboration to ensure any queries of TAT are answered rapidly to ensure an efficient set up process  Collaborate with the Clinical Trial Team to ensure adequate resources are available to conduct the trial  Comply with requirements for consent as outlined in the trial protocol  On call consultant roster for clinical trials  Screen Fails on par with other sites  Actively improve patient care by being a resource to other investigators Business Quality:  Adaptable to the needs of the trial, the Sponsor, and the organisation  Proactively support and mentor other novice principal investigators  Participate in relevant Safety Committees when invited  Perform a formal evaluation of study processes at end of study, with the view to improving efficiency and effectiveness  Undertake the necessary training to maintain your competency as a Principal Investigator, which will be determined by the Learning Management System, each individual trial, and the Good Clinical Practice requirements. Essential  Unrestricted General and/or Specialist Registration with AHPRA  Current Medical Indemnity Insurance  Australian Citizenship or Permanent Residency  Experience working in Clinical Trials  Experience working in a primary care setting  Willing to travel locally and internationally