Posted:1 day ago|
Platform:
On-site
Full Time
Knowledge and Experience: Minimum of 2 years experience in quality assurance, auditing, including sound experience of applicable GxP auditing At least 5 years’ experience in regulatory affairs, clinical research, monitoring, data management, safety/pharmacovigilance, pharmacy, laboratory, or other relevant area in life science such as technology, third party supplier management. Excellent knowledge, understanding and experience of Good Practices (GxPs) and international, national and local regulations and laws related to clinical trials and other clinical research Education: Educated to degree level (technology, biological science, pharmacy or other health related discipline preferred) or equivalent qualification or clinical research experience Master’s degree in a science, technology or industry related discipline, preferred
Parexel
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