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 locally 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