Direct message the job poster from Dimerix Limited
About the role
Dimerix 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 Manager
* Coordination 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/databases
* Oversee the compliance of vendors established plans and quality/performance metrics
* Apply a risk-based quality management system in order to proactively mitigate issues
* Work cross functionally to drive project deliverables with internal and external stakeholders
* Assist with the financial & budget management of clinical studies
* Assist 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 discipline
* A minimum of 2 years of clinical research experience of clinical studies within a pharma company, biotech or CRO
* Clear understanding of current and emerging ICH-GCP work practices and processes.
* Successfully worked with cross functional teams
* Ability to manage key stakeholders across the business and work collaboratively with colleagues from various functional areas
* Demonstrated ability to deliver results to the appropriate quality and timelines
* Experience working on Phase 1 or 2 studies, Phase 3 experience preferable
* Experience in full clinical project lifecycle
* Strong 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 discipline
* Experience working on Phase 3 studies
What we offer
At 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 bonuses
* Professional development opportunities and career progression
* Flexible work arrangements and a healthy work-life balance
If 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:
* Resume
* A separate two paged document addressing the selection criteria
If you have any queries in relation to this opportunity or the application process, please contact Please note applications will not be accepted via this email address.
Applications close: Friday, 14th March 2025
Seniority level
Entry level
Employment type
Full-time
Job function
Management and Manufacturing
Industries
Pharmaceutical Manufacturing
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