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Fusion Clinical Research (Fusion) is a dynamic Phase II-IV clinical trials organisation based at Norwood, SA. Fusion is committed to advancing medical research, enhancing patient care and driving innovation in the healthcare landscape.
Fusion provides an ideal setting for the enrolment of patients with conditions usually managed by their family doctor and an ability to service vaccine trials of all phases.
By partnering with multiple General Practitioners (GPs) and specialists within South Australia, Fusion is able to review GP databases for specific patient populations and inclusion/exclusion criteria to find the right patients for matching trials. Through these established physician-patient relationships, we maintain continuity of care close to patients' homes promoting high participation and trust.
Fusion's Vaccine Arm is experienced in running vaccine trials of all phases and boasts a database of over 8,000 participants, engaged and interested in vaccines to enrol from. This allows Fusion to deliver high throughput vaccine studies and rapid enrolment timelines for a variety of population groups and vaccine targets.
Fusion is a subsidiary of CMAX Clinical Research, one of Australia's largest and most experienced Phase I -II clinical trial units.
About the role:
This is an exciting opportunity in a rapidly growing environment, Fusion is seeking a registered nurse/s to conduct clinical, study-related tasks in line with clinical research protocols and relevant regulations and clinical guidelines.
The Clinical Research Nurse (CRN) reports to the Clinical Research Nurse Team Lead (CRNTL) and supports the Clinical Research and Hub Manager (CR&HM) and Clinical Research Team Leads on daily matters, acting as a resource person for clinic staff.
Responsibilities may include:
Participate in on-study activities as required, including but not limited to:
Collecting blood samples by way of venous cannula or venepuncture at the specified times according to the study schedule, CMAX/Fusion SOPs or protocol requirements;
Administering oral, intramuscular or intravenous medications;
Accurately document the details of blood and urine sample collection in the source data/Case Report Forms (CRFs) in accordance with the Study Protocol requirements in the appropriate manner;
Measure and document vital signs at specified times in the source data/CRFs in accordance with the Clinical Protocol to SOPs or the protocol requirements;
Perform ECG measurements and act appropriately to the results, at specified times according to CMAX/Fusion SOPs or the protocol requirements;
Provide assistance to the physicians when required;
Provide medical care to and monitor the wellbeing of participants;
Perform and/or assist with screening procedures;
Handle and account for the IP;
Document and monitor adverse event reports in accordance with the final Study Protocol;
Ensure safety pathology results are reported, reviewed and followed up in accordance with the Study Protocol or other safety requirements;
Ensure biological samples are processed, stored, shipped and tracked in accordance with the final study laboratory manual;
Control and track study resources in conjunction with the CRNTL ;
Provide assistance and study support to other Fusion Team members.
About you:
We are looking for enthusiastic individuals who can demonstrate meticulous attention to detail to ensure strict adherence to defined study protocols;
You must have current AHPRA registration;
Be competent in basic life support;
Willing to undertake Advanced Life Support training;
Knowledge of, and ability to work successfully within, rigorous standards, protocols and regulations, preferably within ICH GCP;
Well-developed interpersonal skills, including verbal and written communications and negotiation skills;
Ability to provide effective guidance and support to other team members;
Ability to work as an effective member of the Fusion Team and to use initiative and drive to support the CRNTL and other key internal stakeholders;
Demonstrated competence in the personal attributes of initiative, flexibility, time management, working independently and attention to detail;
Proven ability to solve problems in a constructive and evidence-based manner;
Understanding of the principles and practices applying to quality and continuous improvement within a clinical research environment;
Experience in general practice settings is desirable.
Fusion Clinical Research predominantly operates within business hours Monday to Friday.
Successful applicants will be required to attend a mandatory 4-day induction followed by specific training. Training for all clinical assessments will be provided.
If you have experience in clinical trials or are looking for a rewarding career in clinical research, please apply by attaching your application letter and CV via the Apply Now function, applications close on
23 November ****.
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.
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Which of the following statements best describes your right to work in Australia?
How many years' experience do you have as a Clinical Research Nurse?
Are you currently registered with the Australian Health Practitioner Regulation Agency (AHPRA)?
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