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I’m currently supporting an international CRO looking for an experienced Freelance Senior CRA to provide support across an ongoing oncology study in Italy.
This role requires someone who can come into an active study, quickly understand the current status of their sites and work with a high level of autonomy.
The CRA will take ownership of assigned sites and be responsible for maintaining strong relationships with investigators and site teams, ensuring monitoring activities, documentation and follow-up actions are completed accurately and within required timelines.
Key responsibilities:
- Independently manage assigned investigational sites in Italy
- Conduct on-site and remote monitoring activities in line with the study monitoring plan
- Build and maintain strong relationships with investigators, study coordinators and wider site teams
- Complete monitoring visit reports accurately and within agreed timelines
- Proactively manage outstanding site actions and follow-up through to resolution
- Perform source data review/verification and ensure data quality and protocol compliance
- Review essential documentation and support ongoing ISF/TMF completeness
- Identify potential site-level risks and escalation issues appropriately
- Support resolution of data queries, protocol deviations and monitoring findings
- Ensure sites remain compliant with the protocol, ICH-GCP and applicable Italian/EU requirements
- Maintain regular communication with the wider clinical study team regarding site progress, risks and outstanding actions
- Support sites in maintaining ongoing inspection readiness
Requirements:
- Significant CRA/Senior CRA experience within Italy
- Strong and recent oncology clinical xbvzest trial experience is essential
- Previous experience supporting ongoing Phase II/II
📌 Freelance Clinical Research Associate (Italia)
🏢 Hlx Life Sciences
📍 Italia
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