Clinical Quality Assurance Specialist
12 ore fa
Quality Assurance in Clinical Trials
Jefferson Wells is hiring a Quality Assurance Specialist to support a pharmaceutical company in Milano, Italy.
The QA Specialist will ensure that clinical trials are conducted in accordance with current national and international legislation, guidelines, and company standard operating procedures.
Key responsibilities include:
• Development and updating of Standard Operating Procedures for clinical trials to ensure compliance with reference regulations (GCP).
• Planning, coordination, and conducting GCP audits of clinical trials processes.
• Verification of audit reports and certificates in the case of consultant audits.
• Evaluation of corrective action plans and implementation status of corrective and preventive actions.
• Support to internal departments for interpretation of ICH GCP and reference regulations.
This role requires strong knowledge of GCP and quality assurance principles, as well as excellent communication and organizational skills.
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Clinical Quality Assurance Specialist
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Clinical Quality Assurance Specialist
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