Clinical Research Administrator


Company:	Get Staffed Online Recruitment Limited
Salary:	£30,000 to £35,000 a year
Hours:	Full-time
Location:	Bedford, MK44 3UP
Working pattern:	On-site
Job type:	Contract
Posting date:	19 Oct 2026
Closing date:	18 Nov 2026

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Summary

Salary: £30,000 to £35,000 depending on skills and experience + Benefits + Bonus

Location: Bedford

The Vacancy

12-month Fixed Term Contract starting January 2027

Our client is looking for a Clinical Research Administrator to provide support, conduct and monitoring of Clinical studies within the wider Clinical programme ensuring compliance with study protocols and GCP. This will include study preparation, preparation of supplies, volunteer recruitment, study conduct and tracking activities.

Our client are world leaders in the research, design and supply of advanced consumer diagnostic products. They are a joint venture business and their brand is recognised the world over as providing accurate home pregnancy and fertility monitoring tests.

In this role you will be contributing and supporting internal Clinical studies which involves:

- Set-up activities, including sourcing study supplies, packaging and shipment of supplies.

- Tracking study status, inputting into study conduct meetings and reporting of study status.

- Contributing to study administration and execution activities - volunteer recruitment, printing, collation, packing, payment, source data verification and testing.

- Administering and recording volunteer payments for studies.

- Supporting study team meetings and maintaining inspection-ready documentation.

They are looking for individuals who have:

- Good communication skills, both written and verbal, with excellent telephone skills. Previous experience of telephone work is desirable.

- Excellent attention to detail and must be highly organised.

- Good working knowledge of Microsoft 365 (Outlook, Word, PowerPoint and Excel).

- Ideally a Bachelor's Degree in Biomedical Science or a related field.

- Ideally experience with clinical studies.

- Ideally knowledge of IVDR, ISO20916 and ISO13485.

- The personal attributes, attitude and mindset of Results focused, Self-aware and a Team player.

They want you to join them and actively work with colleagues across the business to achieve great things for people in their reproductive life.

Our client can offer you:

- An excellent working environment

- 25 days paid annual leave plus bank holidays

- Company pension scheme including competitive employer's contribution

- Private Medical Insurance package with additional medical cash plan scheme

- Enhanced maternity and paternity pay

- Company supported employee Health and Wellbeing programme

- Life assurance

- Free plentiful car parking and electrical car charging points

- Beautiful parkland setting with excellent transportation links to Cambridge, Milton Keynes and London

Right to Work

All candidates will be asked to provide proof of eligibility to work in the UK at interview.

Due to the requirements laid out by UK Visas and Immigration regarding Right to Work in the UK, our client can only accept applications from individuals who currently have a status allowing them to work in the UK for this position.

They regret that they are unable to offer sponsorship for this role.

Equality

Our client is committed to providing a vibrant, ethical, and sustainable work environment that values equality, diversity, and inclusion.

If you require any reasonable adjustments to support you, at any stage during the application process, just let them know how they can help.

The Company

Our client is a world leader in the research, design and marketing of advanced consumer diagnostic products.

Their research centre is at the cutting edge of innovation and is fully engaged in the development of reliable diagnostic products to empower women on their reproductive journey. They are committed to answering the needs of their existing and future consumers, through a continuous flow of new and innovative products.

Interested?

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