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Meet us at World Vaccine Congress

April 21-24, 2025
Washington USA
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Come and meet us

Our team will be available throughout this event to discuss how we can support your research initiatives. Whether you’re looking to start a new project, save an existing one or simply explore new partnership opportunities, we’re here to help.
Rob Kent

Robert Kent

Senior Director, Business Development

  • Located in West Coast, USA
  • Nurse and healthcare professional
  • Decades of CRO business development experience
  • Deep experience in partnering with medical device, pharmaceutical, and biotechnology companies in USA & Europe

Discover new opportunities and partnerships at World Vaccine Congress Washington, an event uniting the biotechnology and pharmaceutical community.

As a full-service contract research organization, Southern Star Research specializes in accelerating your journey from concept to commercialization. With our experienced team, bespoke solutions and transparent approach, we’re proud to be the Asia-Pacific’s most trusted CRO.

Connect with us at World Vaccine Congress Washington to learn how we can guide you and your product through the complexities of running a clinical trial.

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World Vaccine Congress

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The Australian Advantage

Cost

Eligible organisations receive a 43.5% cash rebate on trial costs with the Australian Research & Development tax incentive.

Speed

Get you trial up and running in 8 weeks with streamlined ethics approvals and no need for an Investigational New Drug application.

Quality

World-class healthcare facilities and renowned experts ensure your data is accepted by international regulatory bodies like the FDA and EMA.
Head Office:
Phone: +61 2 9011 6266

L1, 1 Merriwa Street,

Gordon, NSW, 2072 Australia

E: info@southernstarresearch.com 

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Specialist experience

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.