We have an immediate requirement for our client based in London for a Contract Clinical QA Analyst.

Our client is a fully registered clinical trials unit working across one of the top academic institutes in London. They work to deliver world class trials of all phases in various therapeutic areas.

Brief outline of duties and requirements .

Develop and maintain GCP/ICH compliant processes which control the quality of work and clinical trials including Updating SOP'S

* Actively lead or assist activities in the areas of Internal Audits,
* Lead auditing activities to ensure that studies are conducted in accordance with sponsor protocols, GCP, industry guidelines, agency regulations.
* Lead or assist with identifying non-conformances with requirements, provide suitable recommendations and facilitate ongoing quality improvements using risk-based methodology while maintaining compliance with applicable study protocols, Quality System Regulations and or ISO standards where applicable.
* Assist with management of contract auditors.
* Support special projects requiring QA input. Gap analysis, Changes to Quality Management Systems
* Perform other related duties as assigned.

The Statements made in the job description are intended to describe the general nature and level of work being performed by people assigned to this job.

These statements are not intended to be an exhaustive list of all responsibilities, duties and skills required of people assigned to this job.

Further details will be available upon application.

Please apply if you have immediate availability and include your current CV ,expected Hourly / Daily rate.

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