Description

We have a fantastic new job opportunity for a clinical research professional with an interest in GCP and Quality Management Systems.

You will:

• act as GCP QA Consultant to QRCC clients, providing QA support for clinical development programmes
• manage the Quality Management Systems for QRCC clients
• prepare and maintain core SOPs for clients
• conduct GCP training seminars for QRCC clients
• conduct of QC reviews of essential documents

There is the opportunity for hybrid working and a full benefits package is included.

Requirements

A GCP QA Consultant who has experience working in clinical drug development with direct experience of the establishment and maintenance of Quality Management Systems and of the regulatory environment for drug development is required to expand the existing QA team of a thriving pharmaceutical consultancy company based in St Ives, Cambridgeshire.

As a successful candidate you must be able to think and respond quickly to any given situation and therefore will be expected to demonstrate a common-sense approach, customer service skills, flexibility and an understanding of the firm's business needs.

CANDIDATE REQUIREMENTS

• Robust knowledge of GCP and the regulatory environment for drug development – UK, EU and USA
• Experience working within a clinical drug development environment
• Good administrative, organisational and time-management skills
• Strong IT skills
• Works to a high level of accuracy