Clinical Trial Advisor (4-week contract)
Inner North Brisbane | Immediate start $58–$62 per hour + super
About the role
An immediate opportunity exists for an experienced Clinical Trial Advisor to support a leading research institute on a short-term assignment. This role will suit someone who can step into a complex clinical research environment and provide immediate, high-level operational and governance support across multiple trial activities.
You will be responsible for the effective coordination, monitoring and oversight of clinical trial operations, ensuring alignment with regulatory, ethical and institutional requirements. The role requires a strong working knowledge of Australian and international clinical trial frameworks and the ability to apply these in practice with minimal supervision.
Key responsibilities
- You will provide operational support across all clinical trial activity, including monitoring, tracking and reporting
- A key component of the role will involve strengthening and maintaining monitoring frameworks and contributing to audit readiness and compliance activities
- You will maintain and enhance systems, policies, procedures and training programs that support research ethics and clinical trial governance, including electronic trial master file systems
- You will also review, update and implement policies to ensure they remain aligned with current regulatory requirements and best practice
- The role involves coordination of documentation and content related to research ethics and clinical trials, including procedures and internal resources
- You will support compliance obligations under TGA frameworks, including the Special Access Scheme, and provide advice to internal governance committees as required
- A critical aspect of the position is stakeholder engagement
- You will work closely with researchers, sponsors and internal teams to ensure efficient trial delivery and compliance, while maintaining strong, effective working relationships.
Skills and experience
You hold tertiary qualifications in Science, Nursing, Allied Health, Clinical Research or a related discipline, with demonstrated experience in clinical trials, research ethics or governance. You bring hands-on experience supporting both investigator-initiated and externally sponsored trials, covering study start-up, ethics and governance processes, monitoring, regulatory compliance and ongoing oversight. You have a well-developed understanding of relevant frameworks including NHMRC National Statement, ICH-GCP and TGA requirements such as SAS, CTN and CTA schemes. You have experience working with clinical trial systems and research governance platforms, and can confidently interpret and apply legislation and guidelines. You are familiar with quality assurance processes, audit preparation and maintaining compliance with institutional and regulatory standards. Your communication skills are strong, with the ability to influence and engage a range of stakeholders. You are organised, pragmatic and able to manage competing priorities in a fast-paced environment, while maintaining attention to detail and accountability.
Why apply
This is a short-term, high-impact role within a well-regarded research setting. It offers the opportunity to contribute at a senior level, applying your expertise to support critical clinical trial functions without long-term commitment.
Application
