Senior Clinical Research Associate, Contractor, 0.2 FTE
Location: NSW or Melbourne, Australia only
Engagement: Contractor, part time, approximately 0.2 FTE
We are seeking an experienced Senior Clinical Research Associate to support clinical monitoring activities in Australia on a flexible contractor basis.
This role is expected to be approximately 0.2 FTE, equivalent to around 1 day per week, and would suit an experienced CRA looking for part time contract work alongside other commitments.
The CRA will support monitoring activities in line with study protocols, ICH-GCP, regulatory requirements, and internal procedures. The role may include remote and on site monitoring activity, with occasional travel required.
Key Responsibilities
* Conduct site monitoring visits, remote and on site as required
* Support source data verification and ensure data integrity
* Review clinical trial documentation and support TMF maintenance
* Build effective relationships with investigational sites
* Identify and escalates risks or issues impacting study delivery
* Support site initiation, routine monitoring, and close out activitiesCollaborate with internal clinical operations teams to support smooth study execution
About You
* Previous CRA experience within clinical trials
* Strong understanding of ICH-GCP and clinical trial processes
* Able to work independently with minimal supervision
* Strong communication, organisation, and stakeholder management skills
* Based in NSW or Melbourne, Australia
* Willing to travel occasionally if required
* Life sciences, nursing, pharmacy, or related degree preferred
Please note, this role is only open to candidates currently based in NSW or Melbourne, Australia.
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