Clinical Research Associate (Freelance)

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 , are asked to send their CV. Hays Solutions S.r.l. with sole shareholder. Subject to the direction and coordination of Hays Plc