In sintesi
- Mansioni: Support QA for clinical trials, ensuring safety and data integrity.
- Azienda: Dynamic organization focused on quality in clinical research.
- Benefit: Competitive salary, travel opportunities, and professional growth.
- Altre informazioni: Collaborative environment with significant travel and career advancement.
- Perché questo lavoro: Make a real impact on participant safety and quality culture.
- Qualifiche: Experience in audits, data analysis, and quality assurance.
La retribuzione prevista è compresa tra 72000 - 88000 € per anno.
Overview
In this role you will support QA for clinical trials, ensuring participant safety and data integrity while complying with global regulations.
You will conduct and report on audits, work with cross-functional teams to close QA observations, and apply risk-based approaches to audit planning.
You will leverage data analytics to detect trends and drive continuous quality improvement.
The role offers cross-site collaboration, opportunities to influence quality culture, and significant travel to sites.
- Responsabilità
- Prepare and conduct QA audits and generate audit reports
- Communicate results to QA management and external stakeholders
- Perform risk-based audits using critical-to-quality factors
- Use analytics dashboards and quality metrics to identify trends and prioritize audits
- Collaborate with cross-functional colleagues to drive corrective and preventive actions
- Conduct GCP audits of investigator sites, study level, suppliers, and third parties
- Support scheduling of audits in line with risk assessments with QAL
- Escalate quality issues promptly to QAL and TA Head
- Provide day-to-day QA oversight support to applicable QA functions
- Requisiti fondamentali
- Audits Compliance
- Data Analysis
- Detail-Oriented
- Deviation Management
- Leading by Influence
- Process Improvements
- Quality Assurance Systems
- Quality Risk Management
- Technical Writing
- Ownership and Accountability
- Execution Excellence
- Networking and Partnerships
- Audits Compliance
- Data Analysis
- Detail-Oriented
Sr. Specialist, Quality Assurance datore di lavoro: Merck Sharp & Dohme (MSD)
Lavorare come Sr. Specialist in Quality Assurance presso la nostra azienda significa entrare a far parte di un ambiente stimolante e collaborativo, dove la sicurezza dei partecipanti e l'integrità dei dati sono al centro delle nostre operazioni. Offriamo opportunità di crescita professionale attraverso la formazione continua e la possibilità di influenzare la cultura della qualità, il tutto in un contesto internazionale che prevede viaggi significativi per interagire con team e siti clinici in tutto il mondo.
Dettagli di contatto:
Team di recruiting di Merck Sharp & Dohme (MSD)
