Clinical Auditors Jobs

We handle many vacancies for experienced Clinical Auditors. Below you'll find an example of some typical Clinical Auditors jobs. Login to view our current open positions.

One of the world's largest CROs is actively recruiting within their European quality assurance department. The QA department is moving towards the provision of an auditing service across the full service function and this is an excellent opportunity to move into a varied and challenging r�le. This r�le can be at the senior auditor level for an experienced GCP auditor if appropriate. As an auditor you will be required to travel approximately 50% of your time within Europe to conduct a range of internal and external audits. At the senior level team leadership and development will also form part of your r�le. In return for your commitment and experience an excellent benefits package is on offer including pension, private healthcare, life assurance, car/allowance, 23 days holiday and bonus scheme.

An excellent opportunity to gain auditing experience within the GCP environment! If you are an experienced GLP/GMP auditor or a CRA looking to move into the quality assurance field this is the role for you! Due to recent expansion in the quality operations group our client, a leading provider of drug development services, has an urgent need for auditors to conduct a variety of clinical audits across Europe including site, system, vendor, process and documentation audits. Training will be provided in GCP/auditing processes if required. A competitive remuneration package is available including pension, healthcare, life assurance, 23 days holiday, bonus scheme and flexible working arrangements. Call now to find out more!

Applications are invited from candidates with a good degree and either previous GCP/GLP/GMP auditing experience OR clinical monitoring/project management. Candidates with GLP/GMP only must have at least two years' auditing experience.
Develop your GCP auditing skills! An international drug development company conducting phase II-IV clinical trials in a range of therapy areas has an urgent requirement for an experienced auditor to join their expanding European QA department. This role is partly office based in the South West and will involve 50% travel within Europe to conduct a range of GCP audits: site, system, process, facility, vendor and documentation. Applications welcomed from experienced GMP/GLP auditors with a basic knowledge of GCP.

An exceptional opportunity to become part of a European quality assurance team within a leading biotechnology company! Our client, one of the world's largest biotechnology companies with one of the most promising pipelines in the industry, has an urgent requirement for experienced Clinical Auditors to become part of an established European team. In this r�le you will ensure that all procedures, documents, third party vendors and internal/external facilities comply with regulatory requirements and ICH GCP. You will work on a European level and this will involve liaising with colleagues in the US on quality issues. There is an attractive package available including pension, BUPA, life assurance, stock options scheme, 25 days holiday and personal training scheme. Call today for a confidential discussion about this exciting r�le!

Knowledge of ICH GCP and MCA/FDA/EMEA requirements is essential. To be considered for this r�le you must have a minimum of two years' experience in clinical QA and solid understanding of ICH GCP. Previous experience of site/facility, systems and vendor audits is essential as is involvement with the maintenance and review of quality processes. Previous experience within a biotechnology/pharmaceutical environment is desirable. You will be educated to degree level in a life science and be willing to travel within the UK and Europe as required.

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