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Senior Clinical Research Coordinator

2 weeks ago

Brisbane, Queensland, Australia Paratus Clinical Full time $60,000 - $80,000 per year

Semior Clinical Research Coordinator

Tired of shift work and looking for a change? Interested in gaining experience working in Clinical Trials? Paratus Clinical Brisbane is looking for a full-time Senior Clinical Research Coordinator. The role provides a great balance between clinical and administrative tasks in a variety of clinical research studies. You will be part of a collaborative team that offers flexibility and opportunities to rapidly develop skills and experience.

Paratus Clinical is a network of high-quality private clinical trial sites, established to meet the increasing need for efficient, cost-effective and quality delivery of clinical trials within Australia particularly in the primary care setting. Sitting outside of the Public Health system, we pride ourselves on our responsiveness to client needs with the speed and quality of the delivery of our client's clinical trials. Our mission is to become the provider of choice for many pharmaceutical companies around the world to deliver their clinical trial for new and novel therapies in areas such as vaccine research, dermatology, rheumatology, haematology, asthma, diabetes, pain, high cholesterol, obesity and many more therapeutic areas.

The Role:
The role is full-time and is on-site. However, we are willing to be flexible in terms of hours for the right applicant.

The role includes, but is not limited to the following:

  • Adhere to protocols, ethical and regulatory requirements and GCP guidelines at all times for assigned trials

  • Manage and coordinate participants throughout the study

  • Dispensing and administration of the investigatory product

  • Study-related data entry - source, CRF and site file management

  • Work with the study team, including ethics, recruitment, coordinators and Investigators.

About you:

You must be a team player with excellent communication skills with a strong background in health science or equivalent experience in clinical trials. Having experience using variety of computer applications, databases and electronic medical records. Sharing our values of Resilience, Quality, Responsibility and Collaboration.

Other Essential criteria:

  • COVID19 vaccinated

  • Ability to work independently and as part of a team

  • Exceptional organisational skills and attention to detail

  • Time management skills with the ability to manage a range of clinical research activities, prioritise tasks and meet deadlines

  • Flexible and open to change and excellent problem-solving ability

In addition, the following areas are desirable:

  • Knowledge and understanding of, GCP, regulatory, ethics, privacy and other applicable guidelines

  • Experience working as a coordinator on commercially sponsored clinical trials

To apply send your CV and Cover Letter through the SEEK link.

Applications must be received by COB 13th of June 2025