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 mrinal.murali@dimerix.com. 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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