Clinical Trial Principal Investigator / Sub Investigator at Quiddity Talent Solutions | Torre
Clinical Trial Principal Investigator / Sub Investigator
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Quiddity Talent Solutions

Clinical Trial Principal Investigator / Sub Investigator

Quiddity Talent Solutions
Posted by
Katherine High
Emma
Emma
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Full-time

Legal agreement: Employment

Compensation
AUD200k - 250k/year
~USD139k - 174k/year
Non-negotiable
location_on
Perth, Western Australia, Australia
Posted 3 months ago

Responsibilities

Responsibilities: - Provide clinical oversight for the conduct of clinical trials in accordance with the study protocol, Good Clinical Practice (GCP) guidelines, and regulatory requirements. - Ensure the safety and well-being of all study participants throughout their involvement in the clinical trial. - Oversee the recruitment, screening, and enrollment of eligible participants, ensuring informed consent is obtained and documented correctly. - Manage the administration of investigational products and monitor participants for adverse events or safety concerns. - Maintain accurate, complete, and timely source documentation and case report forms (CRFs) for all study-related activities. - Collaborate with the clinical research team, including study coordinators, nurses, and sponsors, to ensure study milestones are met. - Participate in site initiation visits, monitoring visits, and audits as required by the sponsor or regulatory bodies. - Review and interpret clinical data to ensure the integrity and quality of the trial results. Requirements: - Must be currently based in Perth, Australia. - Must hold current and valid registration with the Australian Health Practitioner Regulation Agency (AHPRA). - Proven professional experience serving as a Principal Investigator (PI) or Sub-Investigator for clinical trials. - Comprehensive understanding of the International Council for Harmonisation (ICH) Good Clinical Practice (GCP) guidelines. - Strong knowledge of local regulatory frameworks and ethical requirements governing clinical research in Australia. - Demonstrated ability to manage complex clinical protocols and adhere to strict study timelines. - Excellent communication and interpersonal skills, with the ability to lead and coordinate multidisciplinary research teams. - High level of attention to detail and commitment to maintaining rigorous data integrity and patient safety standards.
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