
Clinical Quality Assurance Specialist (m/f/d)




Responsibilities
- Support in clinical GCP QA activities
- Development of protocols and review of studies
- Evaluation from the QA perspective
- Creation and review of SOPs in the clinical team
- Pragmatic thinking and innovative problem solving
- Remote and on-site work as required
Profile
- Sound experience in Clinical GCP QA
- Extensive experience (3-5 years) in GDP and clinical activities
- Knowledge of Clinical QA, Clinical Review, Quality by Design
- Fluency in English, other languages an advantage
Benefits
- Flexibility in working hours (30% per week)
- Possibility to work remotely
- Opportunity for personal and professional development
About Hays
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.
Staffing process for freelance specialists
- Analysis of qualifications
- Telephone or personal interview
- Contact with customers
- Contract with Hays
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1. Analysis of qualifications
We carry out a detailed analysis of your technical qualifications on the basis of your CV, your application documents and your profile.
Contact at Hays
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