Principal Investigator

Job Title: Principal Investigator
Location: Melbourne, Australia

Company Overview:
We are partnering with a prominent clinical research organisation dedicated to conducting groundbreaking clinical trials that advance medical knowledge and patient care. With state-of-the-art facilities and a strong commitment to innovation, our client is seeking a highly experienced Principal Investigator to lead clinical trials at their Melbourne site.

Role Purpose:
As the Principal Investigator, you will be at the forefront of clinical research, responsible for the overall conduct of clinical trials. You will ensure the safety of participants, the integrity of the data, and the compliance of the trials with regulatory requirements and Good Clinical Practice (GCP) guidelines. This role is ideal for a dedicated medical professional who is passionate about clinical research and advancing medical science.

Key Responsibilities:

• Oversee the design, implementation, and execution of clinical trials in accordance with study protocols, ethical guidelines, and regulatory requirements.
• Ensure the safety and well-being of all trial participants by monitoring patient care and the effects of investigational products.
• Collaborate with study coordinators, sub-investigators, and other site staff to ensure the successful completion of studies.
• Maintain accurate and complete documentation of all trial-related activities, including case report forms, adverse event reports, and study correspondence.
• Liaise with sponsors, regulatory bodies, and ethics committees to ensure timely approvals and reporting.
• Participate in the recruitment and informed consent process for study participants, ensuring all patients are fully informed about the trials.
• Conduct regular meetings with the research team to discuss trial progress, address challenges, and implement solutions.
• Provide mentorship and guidance to junior investigators and site staff, fostering a culture of excellence in clinical research.

Qualifications & Experience:

• Essential: Medical degree (MBBS or equivalent) with full registration with AHPRA.
• Experience: Minimum of 5 years of experience in clinical research, including experience as a Principal Investigator or Sub-Investigator in clinical trials.
• Desirable: Specialist qualifications in a relevant therapeutic area (e.g., oncology, cardiology, neurology) and experience in conducting phase I-IV clinical trials.

Knowledge & Skills:

• In-depth knowledge of ICH/GCP guidelines, local regulatory requirements, and clinical trial methodologies.
• Strong leadership and management skills, with the ability to lead multidisciplinary teams.
• Excellent communication and interpersonal skills, with the ability to build strong relationships with sponsors, colleagues, and patients.
• High level of attention to detail, with the ability to maintain meticulous records and ensure data integrity.
• Proficiency in using clinical trial management systems (CTMS) and other relevant software.

Why Join?
This is a unique opportunity to lead innovative clinical trials in a supportive and forward-thinking environment. Our client offers a competitive salary, professional development opportunities, and the chance to work on cutting-edge research that has a real impact on patient outcomes.

How to Apply:
If you are an experienced medical professional with a passion for clinical research and are ready to take on a leadership role, we encourage you to apply. Feel free to reach out to Dana Sarkissian on

02 8310 5842 or dsarkissian@i-pharmconsulting.com

Be a part of pioneering research and contribute to the future of medicine!