Clinical Trial Services

We're a full service CRO dedicated to your clinical success.

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Our Process

As a full-service contract research organization (CRO), we have experience supporting a wide range of sponsors in running successful, safe and cost-effective clinical trials.

Whether you need experts in medical writing, clinical monitoring, project management, biostatistics, data management, safety and medical monitoring or quality assurance, our agile and experienced team is ready to help you find a high-quality bespoke solution to meet your needs quickly and at a predictable price.

You can learn more about our team's specific areas of expertise below.

Trust us, we have done it before

Therapeutic Areas

Allergy

Audiology

AutoImmune

Cardiology

Dentistry

Dermatology

Device

Diagnostic

Endocrinology

ENT

Gastroenterology

Gerontology

Haematolology

Healthy Volunteer

Infectious Disease

Intensive Care

Metabolic Disorder

Nephrology

Neurology

Nutrition

Oncology

Oncology - Radiation oncology

Opthalmology

Orthopaedic

Paediatric

Nuclear Medicine

Pain Management

Plastic Surgery

Psychology

Rare Diseases

Respiratory

Rheumatology

Sexual Health

Sleep Medicine

Urology

Vaccine

Vasculopathy

Women's Health

Our Services

Early Phase

Clinical operations

Biometrics

Safety & medical monitoring

Medical writing

Later Phase

Quality Assurance

Study start up

Project management

What our clients say

“I just wanted to send you a quick to let you know that I have been absolutely impressed with the clinical study team, especially with our project manager. They have really stepped up in light of the rush of new patients consenting onto trial and with all the additional work of not being out of study startup yet.
I am so grateful for their hard work!”

Manager, Clinical Operations

Australian, Oncology Biotech (Prostate Cancer)

“I would like to thank you and Southern Star Research team for your great working, as you proactively set the timeline which is about 20 days ahead of the contract defined timeline. There is no doubt that this is the most successful cooperation in my job career.”

Clinical Operations Manager

Chinese Biotech (Healthy volunteer)

“As you know we are now finalizing the signatures of the study reports with global, and I wanted to send you a note on the very good experience I had working with your medical writer on the Part A report. She has always been very responsive, attentive to details and a pleasure to work with. Having had previous (sometimes not that great) experience working with other medical writers, I really wanted to highlight her professionalism.
I would also like to take this opportunity to thank you, and the rest of the team for all your work on this project so far.”

Medical Manager

Multinational Pharmaceutical company (Rheumatoid arthritis)