... Trial Coordinators and clinical admin staff regarding the successful coordination of clinical trials. Key responsibilities will include: Clinical Research Management : Prepare and develop research project documents, including ethics submissions, study ...
... be a key enabler of clinical sites’ success with respect to study enrollment, site relationships, data integrity ...
... be a key enabler of clinical sites’ success with respect to study enrollment, site relationships, data integrity ...
... Islander Studies (AIATSIS) code of Ethics for Aboriginal and Torres Strait Islander Research, The Australian Code for the Responsible Conduct of Research 2018, QUT Code for ... Research Ethics Coordinator, and will receive administrative support ...
... family. UQ Study for Staff. Affordable parking (from just $5.75 a day). Salary packaging options. About You: Relevant tertiary qualifications in Nursing, with a minimum of four years experience as a clinical research nurse coordinator in clinical trials ...
... Islander Studies (AIATSIS) code of Ethics for Aboriginal and Torres Strait Islander Research, The Australian Code for the Responsible Conduct of Research 2018, QUT Code for ... Research Ethics Coordinator, and will receive administrative support ...
... Director OREI and the Human Research Ethics Coordinator, and will receive administrative support ... programs and workshops, and our study assistance scheme. through initiatives such ...
... team members to conduct clinical studies, including operational feasibility, data management ... with an interest in clinical research and drug development. Demonstrated ability ... , and regulatory requirements for clinical studies. Must be willing and possess ...
... tasks allocation phase of the study assigned.Attention to detail.Holds a driver’s license where requiredKnowledge and Experience:Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and ...
... presenting progress reports and study updates. Assist with providing data for reporting on research outcomes, including preparation of abstracts, posters, oral presentations and publications. About You The Clinical Trial Coordinator will be responsible for ...