Operating for more than 30 years, CMAX is Australia's longest running and most experienced clinical trial units conducting successful world‐leading research for local and international clients, specialising in a range of early‐phase trials and first‐in‐human studies.
We are proud to be a key contributor in the advancement of global medicines and technologies - from vaccines and pain control to early warning bio‐devices and hormone replacement therapies, these are just a few of the many research areas for which CMAX has provided clinical trial services.
Employing more than 400 staff, CMAX is a 78‐bed clinical trials unit, with a database of more than 65,000 clinical trial participants, and utilising state‐of‐the‐art facilities, we are primely positioned, opposite the Royal Adelaide Hospital and part of the Adelaide BioMed City precinct.
About the role
The Database Builder configures, deploys and maintains electronic data capture (e-Source) systems for clinical trials, ensuring compliance with SOPs and regulations.
Reporting to the Data Manager, the role involves translating clinical protocols into functional databases and supporting study teams through build, testing and maintenance.
Key Responsibilities
* Develop database specifications from study protocols, lab manuals, and study plans;
* Build and configure study databases (e.g. Medrio/Aero) and eCRFs;
* Ensure data accuracy, integrity and efficient database functionality;
* Implement validation checks and manage updates/amendments;
* Support and coordinate User Acceptance Testing (UAT);
* Troubleshoot issues and escalate complex problems;
* Collaborate with project teams to meet timelines;
* Maintain compliance with regulatory standards (e.g. ICH GCP).
About You
* Tertiary qualifications in science, computing or other relevant discipline are highly desirable but not essential;
* Previous experience with electronic data capture systems (EDCs) typically used in the clinical trials industry would be highly advantageous;
* Strong IT and database configuration skills (including Excel);
* Experience with e-Source systems;
* High attention to detail and strong problem‐solving ability;
* Good communication and stakeholder collaboration skills;
* Ability to prioritise tasks and meet deadlines;
* Able to work independently and in a team;
* Understanding of clinical trial regulations (ICH GCP).
If you are inspired to be a part of a company making a difference in tomorrow's health care and seeking a rewarding career then please apply by attaching your application letter and CV via the Apply Now function, applications close on Sunday 26 April 2026.
Only candidates with approved rights to work full time without restrictions in Australia will be shortlisted for this role.
Please note that we may be conducting interviews during the advertisement period and retain the right to withdraw the advert should we select a successful applicant prior to the closing date.
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