Clinical Research Administrator — 12-Month Contract (Bedford)

Confidential; Bedford; On-site; GBP 30,000 - 35,000; Full time

Benefits offered by this job

25 days annual leave + bank holidays

Pension scheme with employer contrib.

Private Medical Insurance

Enhanced maternity and paternity pay

Health and wellbeing programme

Life assurance

Free car parking and EV charging

Job summary

Swiss Precision Diagnostics GmbH (SPD) is seeking a Clinical Research Administrator in Bedford for a fixed-term 12-month contract starting January 2027. You will support, conduct and monitor clinical studies, ensuring protocol compliance and GCP, including study preparation, supplies, recruitment, and tracking activities.

Key responsibilities include setup of study supplies, tracking status, data entry into meetings, participant payments, and maintaining inspection-ready docs.

Qualifications

• Excellent written and verbal communication skills.
• High attention to detail and strong organisational abilities.
• Proficient in Microsoft 365 (Outlook, Word, PowerPoint, Excel).
• Bachelor-level degree in Biomedical Science or related field preferred.
• Experience with clinical studies and regulatory awareness desired.

Responsibilities

• Set up activities: sourcing study supplies, packaging and shipment.
• Track study status and report through conduct meetings.
• Support study administration: volunteer recruitment, documentation, payments.
• Administer and record volunteer payments for studies.
• Maintain inspection-ready documentation and support study team meetings.

Skills

Communication skills

Attention to detail

Organised

Microsoft 365

Telephone skills

Team player

Results oriented

Self-aware

Education

Bachelor's Degree in Biomedical Science or related field

Tools

Microsoft 365

Job description

Swiss Precision Diagnostics GmbH (SPD) is seeking a Clinical Research Administrator in Bedford for a fixed-term 12-month contract starting January 2027. You will support, conduct and monitor clinical studies, ensuring protocol compliance and GCP, including study preparation, supplies, recruitment, and tracking activities.

Key responsibilities include setup of study supplies, tracking status, data entry into meetings, participant payments, and maintaining inspection-ready docs.