Clinical Trials Coordinator – Oncology Research

Chris O'Brien Lifehouse

Sydney

In loco

AUD 70.000 - 95.000

Tempo pieno

5 giorni fa
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Vantaggi offerti da questo lavoro

NFP salary packaging
Fitness Passport
Employee Assistance program
Onsite gym
E-learning access

Descrizione del lavoro

Chris O’Brien Lifehouse in Sydney is seeking a Clinical Trials Study Coordinator to support the Medical Oncology Department by coordinating trial activities, ensuring protocol compliance, and delivering quality patient care throughout the study. You will liaise with investigators and sponsors, manage recruitment and data, monitor adverse events, and maintain study documentation.

A science or health care degree and at least one year in trial coordination are required; oncology knowledge is

Competenze

  • Degree in science or a health care discipline.
  • Minimum 1 year of experience as a Study Coordinator.
  • Ability to maintain confidentiality and privacy.
  • Immunisations to comply with NSW Health policy for Category A position.

Mansioni

  • Coordinate all aspects of clinical trial operations, ensuring regulatory compliance and study protocols.
  • Facilitate communication between investigators, sponsors and stakeholders.
  • Oversee patient recruitment, screening and enrolment processes.
  • Maintain accurate study documentation and data management.
  • Monitor and report adverse events and protocol deviations.
  • Provide support and guidance to study participants throughout the trial process.

Conoscenze

Study coordination
Regulatory compliance
Communication
Confidentiality
Oncology knowledge

Formazione

Bachelor's degree in science or healthcare

Descrizione del lavoro

Chris O’Brien Lifehouse in Sydney is seeking a Clinical Trials Study Coordinator to support the Medical Oncology Department by coordinating trial activities, ensuring protocol compliance, and delivering quality patient care throughout the study. You will liaise with investigators and sponsors, manage recruitment and data, monitor adverse events, and maintain study documentation.

A science or health care degree and at least one year in trial coordination are required; oncology knowledge is

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