Hiring At UK For Quality Department At Protas - Job Engine

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Tuesday, 24 September 2024

Hiring At UK For Quality Department At Protas


Elevate your career with Protas! Join as GCP Auditor and help enable clinical trials to succeed.

About Protas

Protas is an independent not-for-profit organisation, designing and delivering large, global randomized clinical trials of treatments for common and other life-threatening diseases. Protas is led by the epidemiologist and physician, Professor Sir Martin Landray, who has over 20 years’ experience of leading large, randomized clinical trials as part of a team at Oxford University’s Nuffield Department of Population Health. Most recently, he has been co-leading the landmark RECOVERY clinical trial into treatments for COVID-19 which identified that treatment with the inexpensive steroid drug dexamethasone improved the chances of survival for the most severe cases. It’s an incredibly rewarding place to work where you’ll be surrounded by supportive colleagues who are experts in their own field of excellence. 

We are currently recruiting a GCP Auditor to join our Clinical Operations Team.

About The Role

In this role, you’ll be at the forefront of developing and enhancing our quality audit capabilities within clinical operations and across the entire organization. You will play a crucial part in promoting a culture of quality assurance that aligns with Protas’ mission to deliver excellence.

You will be responsible for planning and executing internal, supplier, and research site audits to ensure compliance with regulatory requirements, GCP, and ISO standards (9001 & 27001). This role also involves conducting root cause analysis, managing and closing out audit findings, and overseeing vendor quality issues to maintain high-quality standards across the organisation.

About you

You will have extensive experience in conducting GCP audits for internal teams, suppliers, and research sites. Additionally, you should possess a strong understanding of scientific research, along with knowledge of the regulatory and policy environment related to clinical trials. Demonstrate in-depth knowledge of clinical trial regulations, GCP guidelines, and other relevant frameworks, as well as their implications for clinical trials.

Additional Information

Protas is committed to being a diverse and inclusive organisation. We strongly encourage applications from people from all backgrounds. For disabled applicants, please contact us to let us know of any adjustments we can make to support you during the recruitment process.

We are currently a primarily remote working organisation but plan to move to hybrid working in the future. We welcome applications from locations across the UK (applicants must have the right to work in the UK). 

We are open to discussions on flexible working arrangements.  

Salary £64,700

Closing date for applications – 7th October 2024

Apply Here


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