Contact us on +44 (0)1270 270010 | info@boydconsultants.com

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Boyds is a fast-growing consultancy business providing a range of expertise and skills central to the development of pharmaceutical and biotechnology medicinal products and medical devices. Based in the UK and Ireland with offices in Cheshire, Cambridgeshire and Dublin, Boyds has an international client base comprising of early-stage life science and medical device companies as well as Universities.

Boyds has earned a reputation for its work in advanced therapies and in 2018, the company was awarded the prestigious Queen’s Award for Enterprise, International Trade for outstanding short-term growth in overseas sales.

Over the last 12 months, the award-winning regulatory team has worked with the regulatory authorities on 19 orphan drug destinations, 11 scientific advice procedures and three investigational new drug applications.

The company’s expertise has also been called on for numerous COVID projects, including two vaccine projects and two therapeutic approaches for the treatment of severe symptoms of COVID-19, as well as setting up and managing clinical trials during the pandemic.

Boyds is also in the process of establishing a US office and we have a separate vacancy open for a US-based Director/Head of Regulatory Affairs. Please see the list of current vacancies on this page for more information about this role and how to apply.

 

 


 

Note to Recruiters: All candidate activity and open positions in the UK and Ireland, are managed through our Head Office in Crewe, Cheshire, therefore, we kindly request that recruiters do not contact employees or hiring managers directly in an attempt to solicit business or present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organisation. Submission of unsolicited resumes prior to an agreement set in place between Boyds and the recruiting agency will not create any implied obligation.

 

Current Vacancies

US-Based Director / Head of Regulatory Affairs

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Programme Management – Director/Associate Director

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Clinical Research Associates

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Associate Director Regulatory Affairs

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