Beschreibung
GCP Auditor - 6 month contract - Frankfurt - €75/hrOptimus Life Sciences are working with a client based in Frankfurt who is in need of a contractor to assist in relieving the work load of their department. The role will be based on site with some flexibility on homeworking for candidates who live in a commutable distance. Experience in auditing early phase clinical trials is essential.
Tasks
- Carry out auditing of early phase clinical studies using QA audit reports.
- Review early phase clinical studies and file the appropriate documentation detailing your findings.
- Maintain QA files and QMS documents.
- Perform regulatory and compliance consulting.
- Further ad-hoc tasks as required.
Requirements
- University Degree in a relevant field.
- 5 years auditing experience in a GCP environment. Additional GLP experience is preferable.
- Expert knowledge of GCP guidelines.
- Experience hosing MHRA and/or FDA audit(s).
- Strong reporting skills.
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