Senior Clinical Trial Coordinator / Clinical Trial Nurse (Casual)
IQVIA
Senior Clinical Trial Coordinator / Clinical Trial Nurse (Casual)
Job Description
Dermatology Clinical Trials | Liverpool NSW | Immediate StartIQVIA is seeking two experienced Registered Nurses to support clinical research activities at a clinical trial site based in Liverpool, NSW.This is an excellent opportunity for nurses with strong Dermatology and Clinical Trial experience who are looking for a flexible casual role within a research-focused environment.About the RoleWorking under the direction of the Principal Investigator and delegated Sub-Investigators, you will support the delivery of dermatology clinical trials and ensure study activities are conducted in accordance with protocol requirements, Good Clinical Practice (GCP) and regulatory standards.This role is casual and study-specific, with approximately 3 hours per week currently required.Key ResponsibilitiesCoordinate study visits and participant communicationsSupport participant recruitment and screening activitiesAssist with informed consent processes under delegated supervisionComplete accurate source documentation and data entryIdentify and escalate adverse events and safety concernsCollect and process biological samples, including venepunctureManage study documentation and regulatory recordsSupport monitoring visits, audits and inspectionsAssist with investigational product preparation, administration and accountability (where delegated)Venepuncture competency, IV administration or infusion competency as requiredEssential RequirementsRegistered Nurse with current unrestricted AHPRA registrationDermatology experienceClinical Trial experienceCurrent GCP Certification, or willingness to complete prior to commencementStrong documentation and organisational skillsAbility to work within study protocols, delegation logs and professional scope of practiceExcellent communication and stakeholder engagement skillsCompliance RequirementsSuccessful applicants will be required to provide:Current AHPRA registrationCurrent GCP Certificate, or ability to complete GCP certification before commencing study-related dutiesCurrent CPR/BLSPolice CheckWorking With Children CheckEvidence of right to work in AustraliaVaccination and health screening recordsRelevant clinical trial experienceWhat's on Offer?Flexible casual engagementApproximately 3 hours per weekWork with a respected clinical research siteOpportunity to contribute to innovative dermatology studiesImmediate start availableApplications are being reviewed immediately. Apply now if you have both Dermatology and Clinical Trial experience and are available to support a growing clinical research program in Liverpool, NSW.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Locations
- Australia, New South Wales, North Sydney
Required Qualifications
- Registered Nurse with current unrestricted AHPRA registration (experience)
- Dermatology experience (experience)
- Clinical Trial experience (experience)
- Current GCP Certification, or willingness to complete prior to commencement (certification)
- Strong documentation and organisational skills (experience)
- Ability to work within study protocols, delegation logs and professional scope of practice (experience)
- Excellent communication and stakeholder engagement skills (experience)
- Registered Nurse with current unrestricted AHPRA registration (experience)
- Current AHPRA registration (experience)
- Current GCP Certificate, or ability to complete GCP certification before commencing study-related duties (certification)
- Current CPR/BLS (experience)
- Police Check (experience)
- Working With Children Check (experience)
- Evidence of right to work in Australia (experience)
- Vaccination and health screening records (experience)
- Relevant clinical trial experience (experience)
- Current AHPRA registration (experience)
- Current GCP Certificate, or ability to complete GCP certification before commencing study-related duties (certification)
- Working With Children Check (experience)
- Evidence of right to work in Australia (experience)
- Vaccination and health screening records (experience)
- Relevant clinical trial experience (experience)
Responsibilities
- Coordinate study visits and participant communications
- Support participant recruitment and screening activities
- Assist with informed consent processes under delegated supervision
- Complete accurate source documentation and data entry
- Identify and escalate adverse events and safety concerns
- Collect and process biological samples, including venepuncture
- Manage study documentation and regulatory records
- Support monitoring visits, audits and inspections
- Assist with investigational product preparation, administration and accountability (where delegated)
- Venepuncture competency, IV administration or infusion competency as required
- Coordinate study visits and participant communications
- Support participant recruitment and screening activities
- Assist with informed consent processes under delegated supervision
- Complete accurate source documentation and data entry
- Identify and escalate adverse events and safety concerns
- Collect and process biological samples, including venepuncture
- Manage study documentation and regulatory records
- Support monitoring visits, audits and inspections
- Assist with investigational product preparation, administration and accountability (where delegated)
- Venepuncture competency, IV administration or infusion competency as required
Benefits
- general: Flexible casual engagement
- general: Approximately 3 hours per week
- general: Work with a respected clinical research site
- general: Opportunity to contribute to innovative dermatology studies
- general: Immediate start available
- general: Flexible casual engagement
- general: Approximately 3 hours per week
- general: Work with a respected clinical research site
- general: Opportunity to contribute to innovative dermatology studies
- general: Immediate start available
- general: Applications are being reviewed immediately. Apply now if you have both Dermatology and Clinical Trial experience and are available to support a growing clinical research program in Liverpool, NSW.
- general: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
- general: IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
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