Services for
Clinical Trials

Delve Medical Writing is an Australian based contract medical writing service that specialises in the development of clinical trial documentation.

An experienced medical writer can assist with the development or review of:

  • Clinical Study Protocols;
  • Clinical Study Protocol Amendments;
  • Clinical Study Reports;
  • Investigator’s Brochures.

Delve works closely with clients, project managers, investigators, study coordinators and biostatisticians as required to produce high quality documents in a timely, cost effective manner.

Delve can assist you with your medical writing requirements on a contract basis as the need arises with processes in place to ensure a confidential, secure and professional service is offered.​

“Mary was a pleasure to work with. The services provided by Delve Medical Writing were very professional, delivering the requested documents within the specified timelines. The communication between the team members and Mary was clear and provided a quick turnaround time with responses.”

Dianne Pepper, Clinical Project Manager, CMAX Clinical Research

"The quality of work has been very good with the responsiveness and turnaround of documents being quick and on time. Always very friendly and professional. Communications have been clear and succinct."

Dr. Tina Soulis, General Manager, Neuroscience Trials Australia

"Mary has been an absolute pleasure to work with. Mary was very patient with us working as a new team for the first time and guided the process seamlessly. The study ran perfectly, in no small part due to the excellence of the protocol preparation and design. Thank you Mary for your professionalism and skill. I can highly recommend Mary and Delve to any organisation requiring excellence in medical writing and a professional who goes above and beyond the call of duty."

Kristina Cabala, Head, Global Clinical Affairs, Reven, LLC

"Writing was of a high quality. The turn around time was exceptional, committing to the timelines we put forward was a big challenge but was achieved with seeming ease. Very professional throughout the process."

Simon Scott, Project Operations Manager, Linear Clinical Research

"It was a pleasure to work with Mary. She is very professional, delivers on time, is flexible, is cost-competitive and client-focused. She repeatedly received excellent feedback from internal team members and the sponsor. We would be happy to recommend her services."

Tanya Zdravkovska, Clinical Project Manager, Andrew Brockway, Associate Business Development Director, IQVIA

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