Clinical Research Coordinator - Nurse/Pharmacist - Full-Time
Tired of shift work and looking for a change? Interested in gaining experience working in Clinical Trials? Paratus Clinical Research Woden is looking for a Clinical Research Coordinator to join our team. 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 Nurse or a Pharmacist with vaccination experience who is a team player with excellent communication skills. Having experience using variety of computer applications, databases and electronic medical records. Sharing our values of Respect and Responsibility, Collaboration, Quality and Safety, and Resilience.
Other Essential criteria
* AHPRA accredited
* 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
* Experience working as a coordinator on commercially sponsored clinical trials
* Knowledge and understanding of, GCP, regulatory, ethics, privacy and other applicable guidelines
* Sample preparation and shipping experience
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