Clinical Trial Doctor, Sub-Investigator – Early Phase Clinical Trial Unit
We are seeking a Sub-Investigator to join an early-phase clinical trial unit in Melbourne. This is a dynamic and exciting role that provides the opportunity to be involved in First-in-Human trials and early-phase clinical research while collaborating with a team of experienced clinical researchers and physicians.
Key Responsibilities:
* Assist the Principal Investigator (PI) in overseeing and conducting early-phase clinical trials, including First-in-Human and Phase I trials.
* Conduct clinical assessments, physical exams, and patient monitoring to ensure safety and efficacy of investigational therapies.
* Manage patient recruitment, including screening for eligibility, obtaining informed consent, and ensuring compliance with study protocols.
* Monitor patients during the trial, reviewing clinical data, conducting adverse event reporting, and ensuring appropriate intervention for any complications.
* Collaborate with the clinical research team to ensure protocol adherence, including pharmacokinetic monitoring, lab tests, and dosing adjustments.
* Participate in study meetings, ethics submissions, and regulatory documentation to maintain compliance with relevant guidelines and regulations.
* Contribute to data collection and analysis, and assist with preparing clinical trial reports, including progress updates for the Ethics Committee and regulatory bodies.
* Support the development of new treatments and therapies, providing insights on patient care and trial outcomes.
* Provide medical oversight to clinical staff and serve as a point of contact for clinical queries during the trial process.
Key Requirements:
* General AHPRA registration (mandatory).
* PGY-3+ with relevant clinical experience.
* Strong interest or experience in clinical research, with a focus on early-phase trials or First-in-Human studies.
* Experience or understanding of pharmacology is preferred, including knowledge of pharmacokinetics and medication management.
* Excellent communication and interpersonal skills to collaborate with multidisciplinary teams.
* Ability to maintain regulatory and ethical standards while ensuring patient safety and trial integrity.
* Strong clinical decision-making and problem-solving abilities in complex and evolving clinical environments.
* Passion for advancing medical research and contributing to the development of novel treatments and therapies.
What’s on Offer:
* 0.6–1.0 FTE flexible working hours.
* A unique opportunity to work alongside leading experts in the field of early-phase clinical research.
* Career development and training opportunities in clinical trials and pharmacology.
* Gain hands-on experience in cutting-edge medical advancements and investigational treatments.
* Work within a highly collaborative and supportive team in an innovative research setting.
* Competitive remuneration with professional development opportunities.
This role offers a fantastic opportunity to gain valuable clinical trial experience in an early-phase research unit and contribute to the advancement of new therapies. If you're passionate about research, pharmacology, and patient care, apply now!
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Health Care Provider, Research, and Science
Industry: Hospitals and Health Care, Hospitals, and Research Services
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