Senior Clinical Trial Coordinator / Clinical Trial Nurse (Casual)

Location: North Sydney and Liverpool, New South Wales, Australia; onsite clinical trial site work in Liverpool, NSW

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Coordinate study visits and participant communications.
• Support participant recruitment, screening, and delegated informed consent activities.
• Complete source documentation, data entry, study documentation, and regulatory records.
• Collect and process biological samples, including venepuncture, and perform IV administration or infusion activities when required.
• Identify and escalate adverse events and safety concerns.
• Support monitoring visits, audits, inspections, and investigational product activities where delegated.

Requirements

• Registered Nurse with current unrestricted AHPRA registration.
• Professional experience in dermatology and clinical trials is required.
• Current GCP certification, or willingness to complete it before commencing study-related duties.
• Strong documentation, organisational, communication, and stakeholder engagement skills.
• Ability to work within study protocols, delegation logs, and professional scope of practice.
• Evidence of the right to work in Australia, current CPR/BLS, Police Check, Working With Children Check, and vaccination and health screening records are required.

Culture & Benefits

• Flexible casual engagement for study-specific work.
• Approximately 3 hours per week currently required.
• Research-focused environment at a clinical trial site.
• Opportunity to contribute to innovative dermatology studies.
• Immediate start available.