Clinical Trial Associate für den Bereich Quality Assurance (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

• Quality Oversight & Systems Management: Monitor compliance with quality guidelines in clinical business areas and implement regional quality plans
• Identify potential gaps, recommend solutions, and escalate relevant issues
• Assist in maintaining and improving quality documents and processes
• Audit & Inspection: Lead and support audit and inspection preparations, including document management and response coordination
• Ensure trial sites and teams are inspection-ready
• Consultation & Collaboration:Serve as the primary quality consultant, providing guidance on regulatory requirements and risk management
• Support root cause analysis, CAPA processes, and audit planning
• Collaborate with quality teams to strengthen quality culture and resolve issues
• Process Improvement & Metrics: Drive continuous improvement and process optimization
• Analyze quality metrics to identify gaps and recommend corrective actions to enhance compliance and efficiency

• Education & Experience: Bachelor's degree in science, technology, or healthcare; experience in quality systems within clinical trials is required
  
• Project Management: Strong ability to prioritize and effectively manage multiple tasks
  
• Communication: Excellent communication skills and ability to influence various stakeholders
  
• Analytical Skills: Problem-solving abilities and attention to detail for risk assessment and process optimization
  
• Teamwork & Flexibility: Independent yet collaborative work style within global teams
  
• Preferred: Experience in a global quality assurance environment and knowledge of regulatory requirements and clinical trial processes
  
• German and Englisch fluent

• Vacation: 30 days
• Work in an international Company

Ihr Kontakt

Referenznummer
821921/1

Kontakt aufnehmen
Telefon:+ 49 621 1788-4297
E-Mail: positionen@hays.de

Anstellungsart
Anstellung bei der Hays Professional Solutions GmbH