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You will be updated with latest job alerts via emailWhen our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
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 Masters degree in a science technology or industry related discipline preferred
Required Experience:
Senior IC
Full-Time