Clinical Trial Associate for the Quality Assurance Department (m/f/d)

Quality Oversight & Systems Management: Monitor compliance with quality guidelines in clinical business areas and implement regional quality plansIdentify potential gaps, recommend solutions, and escalate relevant issuesAssist in maintaining and improving quality documents and processesAudit & Inspection: Lead and support audit and inspection preparations, including document management and response coordinationEnsure trial sites and teams are inspection-readyConsultation & Collaboration:Serve as the primary quality consultant, providing guidance on regulatory requirements and risk managementSupport root cause analysis, CAPA processes, and audit planningCollaborate with quality teams to strengthen quality culture and resolve issuesProcess Improvement & Metrics: Drive continuous improvement and process optimizationAnalyze 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 requiredProject Management: Strong ability to prioritize and effectively manage multiple tasksCommunication: Excellent communication skills and ability to influence various stakeholdersAnalytical Skills: Problem-solving abilities and attention to detail for risk assessment and process optimizationTeamwork & Flexibility: Independent yet collaborative work style within global teamsPreferred: Experience in a global quality assurance environment and knowledge of regulatory requirements and clinical trial processesGerman and Englisch fluent Vacation: 30 days Work in an international Company 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.

Responsibilities

Quality Oversight & Systems Management: Monitor compliance with quality guidelines in clinical business areas and implement regional quality plansIdentify potential gaps, recommend solutions, and escalate relevant issuesAssist in maintaining and improving quality documents and processesAudit & Inspection: Lead and support audit and inspection preparations, including document management and response coordinationEnsure trial sites and teams are inspection-readyConsultation & Collaboration:Serve as the primary quality consultant, providing guidance on regulatory requirements and risk managementSupport root cause analysis, CAPA processes, and audit planningCollaborate with quality teams to strengthen quality culture and resolve issuesProcess Improvement & Metrics: Drive continuous improvement and process optimizationAnalyze quality metrics to identify gaps and recommend corrective actions to enhance compliance and efficiency

Benefits

Vacation: 30 days Work in an international Company