Daniel Evans
Director, Business Development
Director, Business Development
Southern Star Research is heading to the U.S. this June! Join our Director of Business Development, Dan Evans, as he meets with early-stage biotech companies and investors across Salt Lake City and Boston, wrapping up at the BIO International Convention 2025.
This exclusive roadshow is your opportunity to discover how Australia’s clinical trial landscape offers a uniquely stable, cost-effective, and accelerated pathway to early-phase clinical development.
U.S. Roadshow Dates
Why Meet with Southern Star Research:
Why Leading Biotechs Choose Australia for Early-Phase Trials
In today’s uncertain global landscape, biotech leaders are seeking predictability, security, and speed—Australia offers all three.
Book a One-on-One with our Southern Star Research expert
This is your chance to explore how Southern Star Research can help accelerate your clinical development plans while ensuring the security and quality your trial needs.
Whether you’re exploring your first-in-human trial or expanding your global footprint, Australia offers an unmatched clinical trial advantage—and Southern Star Research is your trusted CRO partner on the ground.
Book a Meeting with Dan Evans by submitting the form.
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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.