Job Title

Operating for more than 30 years, CMAX is one of Australias largest, 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-time-in-human studies. These studies have resulted in the advancement of global medicines and technologies, from cancer treatment and pain control to early warning bio-devices and hormone replacement therapies. CMAX operates a 78-bed capacity state-of-the-art facility, we are primely positioned, opposite the Royal Adelaide Hospital and are a part of the growing BioMed City precinct. About the role As a member of the Laboratory Team, the Laboratory Supervisor will provide technical and functional support for the conduct of clinical trial laboratory requirements, in accordance with CMAX Standard Operating Procedures (SOPs) and relevant regulations and guidelines as well as provide laboratory training and support to new and existing laboratory staff. The Laboratory Supervisor will be responsible for The Laboratory Supervisor will act as the laboratory lead from the commencement of a study under the guidance and supervision of the Laboratory Manager. This will involve assisting in a range of studyspecific set up duties as required, coordinating and maintaining the sample shipping calendar and coordinating and documenting laboratory equipment maintenance activities. In addition, the Laboratory Supervisor will provide effective handson support to laboratory staff members, provide additional training (as required) and may be responsible for (but not limited to): Assisting with the induction and onboarding of new staff to the laboratory; Administering and overseeing the laboratory training program; Coaching to meet skills gaps and needs as identified; Providing ongoing laboratory training and studyspecific training for staff; Assist in reviewing and updating SOPs and WIS; Plan, prepare, coordinate and meet studyspecific requirements and deadlines; Reviewing sample processing manuals for new studies; Drafting sample processing protocols as required by the study protocol; Ordering studyspecific supplies; About you Tertiary qualifications in a science or health care discipline are desirable; IATA Certificate is desirable (if not already held, ability and willingness to pass the certificate is mandatory); Demonstrated general knowledge of the standards, procedures and regulations relating to the conduct of clinical studies including ICH GCP is desirable; Demonstrated competence in general laboratory practices and biological sample handling; Ability to provide support and assistance to a small team committed to achieving high quality outcomes for internal and external customers; Experience in training individuals and small teams; Experience/knowledge in developing training content and materials; Effective interpersonal skills, including verbal and written communication skills and the ability to liaise/consult with a diverse range of staff and stakeholders; Proven ability to follow specific instructions, work within rigorous standards, protocols and regulations and apply high attention to detail; Demonstrated understanding of GCP and GLP principles; Proven ability to work independently as well as collaboratively with peers, colleagues and other team members; Note: Laboratory work at CMAX does not involve any diagnostic or bioanalytical analysis on-site. If you are interested in this opportunity, then please apply by sending your application letter and CV via the Apply Now function, applications close on Sunday 22 March 2026. Only experienced 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. #J-18808-Ljbffr