Green Lane Coordinating Centre Limited (GLCC) is an Academic Research Organisation (ARO) formed by personnel working at the world-renowned Green Lane Hospital now Greenlane Clinical Centre in Auckland, New Zealand.

During the three decades since GLCC’s inception, our leadership has developed key relationships with investigative sites in New Zealand and the Asia-Pacific region. These relationships span many therapeutic areas including Cardiology, Endocrinology, Obstetrics and Gynaecology, Neurology & Integumentary disease.

GLCC works closely with a core group of investigators in New Zealand, Australia, Singapore, Hong Kong, Malaysia, Thailand, Korea & the Philippines to deliver high quality data in compliance with the United States Food and Drug Administration (FDA) Code of Federal Regulations.

At GLCC, it is our highly trained team that ensures we deliver quality clinical trial solutions to our clients on every project we undertake. Our motivated and experienced team truly are our biggest assets.

The team, based both in New Zealand and Australia, consists of Clinical Trial Managers, Project Managers, Clinical Research Associates, Regulatory Affairs specialists, Clinical Trial Assistants and Administrators who work with our leadership in a supportive and collaborative environment.

Our well-established quality systems and experience with regulatory agencies such as the New Zealand Ministry of Health – Medsafe Division and the Health and Disabilities Ethics Committees, ensures our regulatory submissions are completed, reviewed, processed and obtained in a timely and professional manner.

Together with support from national and international academia, we are dedicated to achieving the highest possible standard in clinical research.GLCC’s unique structure provides a diverse and expanding network of national and international resources including scientific collaboration, practical clinical expertise and academic partnerships.

We believe our unique combination of local knowledge, experience and partnerships is the vital ingredient to provide our sponsors with an efficient, professional and cost-effective clinical trial solution. Ensuring our sponsors expectations are met.


  • Clinical expertise, scientific partnerships and academic collaborations
  • Cost efficiency
  • Ability to select appropriate sites / investigators
  • Quick turnaround time for completion of regulatory documents
  • Implementation of recruitment and retention strategies
  • Ensuring integrity of research data and study conduct
  • Well established relationships with investigators both nationally and internationally
  • In-depth knowledge of local and international regulatory requirements
  • Efficient and effective communication and logistics pathway
  • Setting realistic and achievable recruitment targets
  • Timely site activation and start up
  • Ensure contractual framework reflects intent
  • Provide feedback communication ow and flexibility within the program
  • Dedication and commitment