Senior Oncology Research Nurse
vor 1 Monat
Location: Sydney, CBD, Inner West & Eastern Suburbs
Industry: Healthcare & Medical, Clinical/Medical Research
Nursing – High Acuity (Healthcare & Medical)
Position: Full time
Join the Scientia Clinical Research (SCR) team State-of-the-art early phase clinical research facility located in The Bright Alliance Building, Randwick, NSW.Multi-functional team of Medical, Clinical, Nursing, Pharmacy, Laboratory, Quality and Data Management professionals. Highly experienced in the early development of new primarily in immunotherapy and targeted therapy.A Not For Profit Organisation offering salary packaging benefit entitlements.We are seeking a highly skilled and experienced Senior Oncology Research Nurse to join our dynamic team dedicated to advancing cancer research and patient care. As a Senior Oncology Research Nurse, you will play a pivotal role in overseeing and managing early phase (1/2) oncology clinical trials, ensuring the highest standards of patient safety, care, and data integrity. You will work closely with a multi-functional SCR team of oncologists, nurses, pharmacists, clinical project managers, clinical study co-ordinators, data managers, the study Sponsor teams and clinical research associates.
Your responsibilities will encompass protocol review, engagement in sponsor communication, and the continual enhancement or maintenance of trial quality.
About Scientia Clinical Research Scientia Clinical Research (SCR) is the first publicly funded purpose-built early phase clinical trials centre in NSW. Located in the Bright Alliance Building with the Nelune Comprehensive Cancer Care Centre and services of the Sydney Children's Hospital. Co-located in a major research precinct with Prince of Wales Hospital, Royal Hospital for Women, UNSW Sydney and the Lowy Cancer Research Centre.
About you To be successful for this position you will fulfil the following criteria:
Registered Nurse with recent experience in oncology nursing.Experienced in oncology clinical procedures, treatments and patient assessment techniques (e.g. administration of chemotherapy and/or immunotherapy, care and management of Central Venous Access Devices, and Cannulation).Good working knowledge of clinical research, ICH GCP and the basics of drug development is desirable.Must have experience in Phase 1 setting.Excellent written and oral communication skills to communicate and collaborate with a wide range of stakeholders in a multidisciplinary framework.Self-motivation, pro-activity and an interest in clinical research.Excellent planning and organisational skills and ability to multitask.Commitment to quality and excellent attention to detail.Ability to be flexible in working hours if required.Competent with the use of Microsoft Word, Excel and PowerPoint.World-class clinical trial expertise and state-of-the-art facilities.
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