Senior Clinical Research Nurse Coordinator

Paratus Clinical; Canberra; On-site; AUD 90,000 - 120,000; Full time

Job summary

Paratus Clinical Research Canberra is seeking a Senior Clinical Research Nurse Coordinator to join our on-site team in Canberra. This full-time role balances clinical duties with essential trial administration in a supportive, collaborative environment.

You will adhere to GCP, regulatory and ethical standards, coordinate participants, manage data entry and assist with study materials, working closely with ethics boards, recruitment teams and investigators.

Qualifications

• Must be a registered nurse with AHPRA.
• 2–3 years' experience as a Lead Clinical Trial Coordinator.
• Experience with GCP, regulatory, ethics and privacy guidelines.
• Strong organizational and time management skills.
• Excellent communication and teamwork abilities.

Responsibilities

• Adhere to protocols, ethical and regulatory requirements and GCP guidelines for trials.
• Manage and coordinate participants throughout the study.
• Preparation, dispensing and administration of investigational products.
• Study-related data entry - source, CRF and site file management.
• Collaborate with ethics, recruitment, coordinators and Investigators.

Skills

Nursing

Communication skills

Teamwork

IT literacy

Attention to detail

Education

Nursing Registration (AHPRA)

Tools

Electronic Medical Records (EMR)

Databases

Job description

Senior Clinical Research Nurse Coordinator

Senior Clinical Research Nurse Coordinator - Full Time

Tired of shift work and looking for a change? Interested in gaining experience working in Clinical Trials? Paratus Clinical Research Canberra is looking for a Full-Time Clinical Research Nurse 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.

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
• Preparation, 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 and 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:

• 2–3 years' experience as a Lead Clinical Trial Coordinator.
• Nursing AHPRA Registration
• Mental Health Experience
• 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 as blinded/unblinded on commercially sponsored clinical trials
• Knowledge and understanding of, GCP, regulatory, ethics, privacy and other applicable guidelines
• Sample preparation and shipping experience

Applications must be received by 11:59pm AEST Friday 20 November 2026.

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