Tasman Oncology has a FULL-TIME Clinical Research Coordinator (1 year fixed term contract) position available for an experienced, highly motivated, efficient, and well-organized Clinical Research Coordinator to join our research-focused oncology clinic located in Southport. Our Coordinators are rewarded with stimulating work, a supportive multi-disciplinary team, and full training for the position. You will spend part of your time in our clinic with patients, with the remaining time spent performing clinical trial documentation, data entry, and sponsor/vendor liaison.

This is a challenging but rewarding role, as we seek to develop new cancer therapies and make a difference in the lives of cancer patients. Our ideal candidate:

The Clinical Research Coordinator will have a medical/health science or closely related science degree. They will demonstrate excellent time management and organizational skills, a high level of communication and interpersonal skills, and meticulous attention to detail.

Experience as a Clinical Research Coordinator will be highly regarded. Job tasks and responsibilities

Key responsibilities

Work with the Principal Investigator (PI) to manage the day-to-day activities of a clinical trial including problem-solving, communication, and protocol management.

Build rapport and liaise with patients on your clinical trials

Performing clinical procedures, including health questionnaire assessments and ECGs (full training provided)

Performing laboratory processing of specimens





Organizing patient appointments and procedures

Ensuring informed consent is obtained and stored

Preparation and maintenance of study documents for the implementation of a clinical trial

Completion of data entry, data queries, & quality assurance checks

Liaising with Clinical Research Associates and Sponsor Representatives

Coordinating a number of studies simultaneously

Pro-actively providing ongoing information to management to ensure key milestones remain on-track

Tracking and proactively following up on any adverse events

Preparation and submission of regulatory documents for Ethics Committee Review

Ensuring studies are conducted in accordance with regulatory and ethical guidelines, as well as Tasman Oncology Research Standard Operating Procedures Skills and experience

Mandatory

Bachelor's degree in relevant health sciences (medical) or allied health field (medical):

Solid verbal and written communication and interpersonal skills; to develop customer relationships, manage customer issues sensitively and assertively, capability to provide and receive positive and negative feedback

Attention to detail and proactive nature

Time management skills with the ability to manage a complex portfolio of clinical research activity, prioritize tasks and meet deadlines

Desired

Minimum 2 years experience in the coordination of clinical research

Medical oncology knowledge, skills, or experience

Applied Good Clinical Practice training

📌 Clinical Trial Coordinator (Gold Coast)
🏢 Tasman Health Care
📍 Gold Coast