Chris O’Brien Lifehouse is an internationally recognised independent, not-for-profit cancer hospital leading the way in delivering patient-centred cancer care. We seek passionate, caring, and dedicated staff who align with our Founder’s vision of creating a team-oriented environment in which, respect, discovery, empowerment, and nurture, thrive in the interests of our patients.
About the role:
The Clinical Trials Study Coordinator assists with the effective and timely management of clinical trials research activities of the Medical Oncology Department, including the management and provision of quality care of patients participating in clinical trials, conducting protocol requirements and monitoring study protocols.
Coordinating all aspects of clinical trial operations, ensuring compliance with regulatory requirements and study protocols
Facilitating communication between investigators, sponsors, and other stakeholders
Overseeing patient recruitment, screening, and enrolment processes
Maintaining accurate and up-to-date study documentation and data management




Monitoring and reporting adverse events and protocol deviations
Providing exceptional support and guidance to study participants throughout the trial process

Essential Criteria:
Degree in science or a health care discipline
Proven experience in a clinical trials workplace in an acute setting
Ability to maintain and always understand the importance of confidentiality and privacy
EDC (Electronic Data Capture) systems i.e. iMedidata RAVE, InForm etc. - Desirable
Medical oncology knowledge, skills, or experience - Desirable
Evidence of immunisations to comply with the NSW Health Occupational Assessment, Screening & Vaccination against Specified Infectious Diseases Policy for a Category A position

Advantages
Optional NFP salary packaging – increase your take home pay with $15,900 tax free benefit + meal and entertainment card.
Fitness Passport Access.
Employee Assistance program.
Ons

📌 Study Coordinator Prayagraj
🏢 Chris O'Brien Lifehouse
📍 Prayagraj