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Your complete clinical trial study start up checklist

Your must-have clinical trial checklist to ensure your study kicks off to a smooth start. 

Clinical trial startup can be challenging. It demands precise coordination among stakeholders, detangling the regulatory web, and the know-how for engaging appropriate sites with the necessary infrastructure.

This makes it difficult to keep tabs on all the essential steps for an efficient and compliant start up. So, we’ve done the hard yards for you with our ultimate clinical trial study start up checklist.

Underpinned by years of clinical experience, we demonstrate how to optimize each step of the clinical trial implementation process.

Download the clinical trial checklist to uncover:

  • How to minimize delays and set your trial on a clear path for success.
  • How to ensure your clinical trial is feasible and that you engage the right study sites.
  • How to choose the best CRO with specific experience for your clinical study.

Don't let the challenges of trial startup hold you back—take control and make informed decisions. Your study success awaits; get started today.

Download the checklist

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Gordon, NSW, 2072 Australia

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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.