Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.
Key responsibilities
Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs
Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information
Maintain accurate documentation including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements
Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management and client-facing meetings
Coordinate (working with the RN team) and complete subject trial visits on- and off-site.



Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately
Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs
Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents
Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for those patients for on- and off-site care
Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required
Report any suspected misconduct or fraud to Illingworth and associated companies
About you
Registered nurse with a minimum of 2 years' post qualification experience
Research and clinical trials experience with GCP certification
Knowledge of research design and methodology desirable
Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable
Ability to work autonomously with initiative in a team within a multidisciplinary environment
Excellent verbal and written communication skills
Ability to prioritize and manage multiple tasks
Positive working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum
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📌 Casual Research Nurse (Melbourne)
🏢 Syneos Health
📍 Melbourne