We are seeking a highly skilled Clinical Research Coordinator to join our team in the Department of Cardiology. The successful candidate will be responsible for planning, initiating, and conducting clinical research studies within the department.
Job Description
* The primary purpose of this role is to manage a caseload of patients participating in trials within the research portfolio of Senior Cardiologist, Professor Geoffrey Tofler.
* Under the supervision of the Principal Investigator and the Senior Research Coordinator Cardiology, the Clinical Research Coordinator will plan, initiate, and conduct clinical research for the Triggered Acute Risk Prevention (TARP) Study.
* This exciting new clinical trial will evaluate a strategy which empowers individuals to recognise stressors (triggers) and respond appropriately to reduce cardiovascular disease (CVD) risk.
Responsibilities
* Ensure the research is conducted in accordance with protocol, policy, legislation, ethical requirements and guidelines for evidence-based clinical practice to achieve high-quality data for research.
* Collaborate with the research team to develop and implement research protocols, case report forms, and other study-related documents.
* Conduct patient assessments and interventions as required by the study protocol.
* Maintain accurate and detailed records of patient interactions, including consent forms, adverse event reports, and study completion status.
Requirements
* Current registration as a Registered Nurse with the Australian Health Practitioner Regulation Agency (AHPRA) with at least 3 years' experience working as a Registered Nurse.
* Experience in or working knowledge of clinical research, including the conduct of clinical trials.
* Experience in or working knowledge of research ethics and governance approval processes, GCP guidelines, the National Statement on Ethical Conduct in Human Research and associated legal and regulatory guidelines as it relates to the conduct of research in the NSW public health system.
* Good written and verbal communication skills to facilitate interaction with a range of stakeholders such as clinical trial sponsors, patients/participants, study investigators and other clinical trials staff.
Benefits
The successful candidate will have the opportunity to work in a dynamic and collaborative environment with a dedicated research team. The position offers a competitive salary and benefits package, as well as opportunities for professional development and growth.
The ideal candidate will possess excellent communication and interpersonal skills, with the ability to work effectively in a fast-paced environment. They will also have a strong understanding of clinical research principles and practices, as well as the ability to work independently and collaboratively as part of a team.