Danaher Corporation
Danaher Corporation
Danaher Corporation ilmiy tadqiqotlar, biotexnologiya va klinik sinovlarda qo‘llaniladigan hayot fanlari hamda diagnostika texnologiyalarini ishlab chiqadi. Kompaniyaning biznes yo‘nalishlari akademik muassasalar, farmatsevtika va biotexnologiya kompaniyalari, shuningdek klinik laboratoriyalar uchun asbob-uskunalar, dasturiy ta’minot, texnologiyalar va xizmatlarni taqdim etadi. Kompaniya biotexnologik vositalar, diagnostika platformalari va hayot fanlariga oid boshqa mahsulotlarga e’tibor qaratadi, faoliyatini Danaher biznes tizimi orqali boshqaradi hamda texnologik portfeli va mijozlar qamrovini kengaytiradigan xaridlar orqali rivojlanadi.

Clinical Compliance Auditor

Support clinical and vendor audits, NMPA inspections, and compliant clinical processes as a Clinical Compliance Auditor. Danaher helps customers worldwide address complex challenges in science and technology.

Tavsif

  • Coordinate internal and external audits.
  • Help develop annual audit programs and schedules.
  • Lead or support site and sponsor clinical audits.
  • Evaluate clinical study compliance with applicable standards and regulations.
  • Prepare and distribute audit schedules, plans, and reports.
  • Review objective evidence and classify nonconformity findings.
  • Monitor audit findings and corrective actions through documented completion.
  • Create and maintain clinical and quality metrics.
  • Participate in NMPA inspections.
  • Manage vendor and supplier qualification from initiation through completion.
  • Develop compliant clinical processes.
  • Maintain and revise processes, procedures, and SOPs.
  • Help train Clinical Affairs staff on regulations, standards, requirements, processes, best practices, and SOPs.
  • Support clinical study teams and resolve clinical compliance issues.
  • Work with customers and global teams to address complex challenges and advance science and technology.

Talablar

  • The source does not specify particular clinical compliance auditing qualifications or experience.
  • Working knowledge of applicable clinical standards and regulations.
  • Familiarity with NMPA inspections.
  • Ability to perform site, sponsor, vendor, and supplier audits.
  • Ability to qualify vendors and suppliers and conduct risk assessments.
  • Ability to develop and maintain clinical processes, metrics, procedures, and SOPs.
  • Ability to support clinical study teams and resolve clinical compliance issues.

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