Direct message the job poster from Dimerix LimitedAbout the roleDimerix is seeking a talented Clinical Project Associate to join our team based in Fitzroy, VIC. This is a full-time position reporting to the Clinical Project Manager that will play a vital role in supporting the execution of our clinical trial activities. As a Clinical Project Associate, you will be responsible for providing operational and administrative support to ensure the seamless and efficient delivery of our clinical research projects.Key Responsibilities:Supports and facilitates the planning and execution of clinical studies on time, adheres to required quality standards and within budget in collaboration with the Clinical Project ManagerCoordination of the clinical studies activities to ensure key milestones, project timelines & deliverables are met during study start-up, delivery and close out.Support the Clinical team in the management and oversight of CROs to develop and maintain strong, collaborative relationships with key internal and external stakeholders.Support development of key study documents/databasesOversee the compliance of vendors established plans and quality/performance metricsApply a risk-based quality management system in order to proactively mitigate issuesWork cross functionally to drive project deliverables with internal and external stakeholdersAssist with the financial & budget management of clinical studiesAssist with integration of clinical studies supply and logistics processes.Ensure study is conducted in accordance ICH/GCP standards & regulatory requirements.What we're looking for:University degree or equivalent in a related science or healthcare disciplineA minimum of 2 years of clinical research experience of clinical studies within a pharma company, biotech or CROClear understanding of current and emerging ICH-GCP work practices and processes.Successfully worked with cross functional teamsAbility to manage key stakeholders across the business and work collaboratively with colleagues from various functional areasDemonstrated ability to deliver results to the appropriate quality and timelinesExperience working on Phase 1 or 2 studies, Phase 3 experience preferableExperience in full clinical project lifecycleStrong project oversight & organisational skills in overseeing studies and ensuring that all aspects & documentation are attended to with a high level of attention to detail.Excellent interpersonal and communication skills with the capacity to communicate with individuals across disciplines and at all levels in the organisation.Demonstrated ability to work both independently and harmoniously as part of a small agile multidisciplinary team.Higher degree in a related science or healthcare disciplineExperience working on Phase 3 studiesWhat we offerAt Dimerix, we are committed to creating a supportive and inclusive work environment that empowers our employees to thrive. We offer a range of competitive benefits, including:Generous remuneration and performance-based bonusesProfessional development opportunities and career progressionFlexible work arrangements and a healthy work-life balanceIf you're passionate about making a difference in the healthcare industry and are looking to join a dynamic, innovative team, we encourage you to apply for this role today.Join Us!If this sounds like your next role, please click APPLY NOW and provide the following documents:ResumeA separate two paged document addressing the selection criteriaIf you have any queries in relation to this opportunity or the application process, please contact mrinal.murali@dimerix.com. Please note applications will not be accepted via this email address.Applications close: Friday, 14th March 2025Seniority levelEntry levelEmployment typeFull-timeJob functionManagement and ManufacturingIndustriesPharmaceutical Manufacturing
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