WHO WE ARE

Vial Australia Pvt Ltd is the Australian arm of Vial, a cutting-edge clinical research organization dedicated to advancing innovative therapeutics through efficient clinical trials. Vial Australia leverages local expertise and infrastructure to conduct high-quality clinical trials for Vial’s extensive drug portfolio.
Our mission is to bring transformative medicines to patients by executing world-class clinical research in Australia. We combine Vial’s innovative approach to clinical trials with Australia’s robust regulatory framework and experienced clinical research community.
Vial Australia Pvt Ltd operates as a key strategic partner in Vial’s global clinical development programs, providing access to Australia’s diverse patient populations and streamlined regulatory pathways. We are committed to maintaining the highest standards of clinical research while accelerating the development of life-changing therapies.

WHAT YOU’LL DO

We are seeking a Gastroenterologist to join our clinical trial team as a Sub-Investigator / Independent Clinician (or in a supporting capacity to the Principal Investigator) for a study in patients with Inflammatory Bowel Disease (IBD).
This is a unique opportunity to contribute clinical expertise to a First-in-Human (FIH) study involving a monoclonal antibody, playing a pivotal role in ensuring patient safety, scientific integrity, and adherence to regulatory standards.

KEY RESPONSIBILITIES

• Perform and/or oversee study-specific procedures, including endoscopies at protocol-defined timepoints
• Support the Principal Investigator in all aspects of trial conduct, including protocol adherence, patient safety oversight, and data integrity
• Assess and monitor patient safety, manage adverse event reporting, and ensure prompt escalation of safety concerns
• Collaborate with the research team, study coordinators, and site staff to ensure smooth execution of study visits
• Review and sign off on source documentation, case report forms, and other trial-related documents in compliance with ICH-GCP standards
• Participate in investigator meetings, monitoring visits and more as required
• Contribute medical expertise to discussions with ethics committees, sponsors, and regulators where applicable