
Teresa Ringeri
Director – Strategy Coordination

Director – Strategy Coordination

Head of Site Liaison

Study Start Up Specialist
Southern Star Research is proud to participate in the SCRS Australia & New Zealand Site Solutions Summit™ 2025 – a premier gathering where sponsors, clinical research organizations (CROs), and solution providers unite to share insights and build connections to shape the future of clinical research in this region.
As a full-service Australian CRO with a strong local and global presence, Southern Star Research delivers customized support to early-phase biotech companies seeking to grow, scale, and attract investment. Whether you’re an emerging biotech, investor, or a financial advisor, our team welcomes you to connect and collaborate.
Why Meet with Southern Star Research at SCRS ANZ 2025?
What You’ll Gain from the Summit
Join over 500 attendees from 250 organizations and hear from 80+ expert speakers at this leading event focused on advancing clinical trials across Australia and New Zealand. The summit offers valuable insights and practical discussions to help you navigate today’s clinical research landscape.
We look forward to seeing you in Melbourne.
Connect with our experts from July 22-23 at the SCRS Australia & New Zealand Site Solutions Summit™ 2025 to discuss new clinical research initiatives and innovations. Fill out the form below to schedule a meeting with our team.
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L1, 1 Merriwa Street,
Gordon, NSW, 2072 Australia
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Each member of our Leadership Team boasts an average of 30 years experience. Our clients have access to an extraordinary group of Clinical Research professionals, whose experience covers Multinational Pharmaceutical companies, Biotechnology, Medical Device, CRO’s, research institutes, Universities, Industry Associations & Government Bodies. Together, we ensure that every aspect of your unique and novel drug study clinical trial is handled with scientific precision, care, and foresight.
Our team has all of the tools, knowledge and experience to solve almost any issue that may arise during the complex clinical trial process.
We recognize that each study is unique and different and there are nuances that need to be resolved proactively.
Our advisory board of top-tier specialists in multiple therapeutic areas engage in the early stages from protocol design in constructive discussions to anticipate challenges and enhance study efficiency throughout the study.