Gcp Auditor Home-based
hace 2 semanas
GCP Auditor
Our Client, which is one of the leading consultancy companies in the field of quality assurance, is offering a role of a GCP Auditor.
**In this role, you will**:
be planning and conducting GCP audits (vendor, internal process and investigator site);
act as a Subject Matter Expert (SME) for clinical-related projects;
be independently managing clinical-related audits and providing consulting and contract services to clients;
contribute to designing, implementing, monitoring and maintaining QMS processes, policies and strategies and ensuring company compliance with GCP regulations, internal procedures and policies in cooperation with peers.
**Requirements**:
Hands-on experience in Clinical Research, e.g., as CRA, monitor, and trial project manager.
Minimum 5 years of experience in a GCP environment.
Experience in other GxP areas is an advantage
3 years of experience in an international GCP quality assurance role, including leading GCP audits, will be an advantage.
Ability to interact in a professional and positive manner with clients and co-workers.
High level of understanding of international GCP requirements and standards in the pharmaceutical, medical device and biotech industries.
**Benefits**:
Competitive salary and attractive company bonuses
Home-based role - work from anywhere located in EU
Diversified tasks - you will not be overloaded with routine
Travelling globally - get global experience in the field - especially suitable for those ones passionate about travelling
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