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Our client is an international CRO that provides complete clinical trials management support for diverse therapeutic areas, such as oncology, cardiology and medical devices. Their vision is to become the preferred CRO for life science companies across the world. This is a great opportunity for someone looking for growth and an exciting challenge. Job Responsibilities: 1) Assist the management with overall quality, compliance and auditing activities 2) Ensure compliance of operations with corporate policies, industry standards and applicable regulations by conducting audits of internal files, clinical sites and vendors used to support clinical trials 3) Support organizations GCP mentoring and compliance by ensuring quality activities are performed and documented in compliance with SOPs
Details :
- company: Sterling-Hoffman Life Sciences
- employee_type: Full Time
- full_time: Full Time
- industry: Automotive,Accounting & Finance
- job_title: Auditor,QA
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