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