Your new company
Our client is a leading company in the Pharma Sector.
We are seeking a Senior Clinical Research Associate to join our team
You new role
* Ensure compliance with client SOPs, study protocols, ICH-GCP and applicable regulations
* Train and support investigator site teams on study procedures and systems
* Conduct site initiation, monitoring (on-site and remote), and close‑out visits
* Verify informed consent, study material management, and biological sample handling (if applicable)
* Monitor data accuracy and quality by verifying eCRF data against source documents
* Review and ensure proper reporting of adverse events (AEs/SAEs)
* Maintain investigator site files and manage essential regulatory documentation
* Prepare visit reports and follow up on action items with site teams
* Provide technical support for eCRF systems and data entry
* Maintain regular communication with investigators and project teams
* Support patient recruitment and investigator engagement
* Manage study archiving and support site billing processes
* You will be involved in the IRB submission process (for linguistic support).
Requirements:
* Required experience level: Ideally experience in ATTR cardiac amyloidosis and in non‑interventional studies. If this is not possible, we search for a confirmed/senior CRA.
* At least 10 years experience in the role and functions describe above.
What to do now
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Candidates of both sexes, after having read the mandatory privacy information on the website www.hays-itservices.it, are asked to send their CV. Hays Solutions S.r.l. with sole shareholder. Subject to the direction and coordination of Hays Plc