Clinical Trial Assistant
Role Overview
Join Panthera Biopartners as a Clinical Trial Assistant at its Preston clinical research site.
This is a 12-month fixed-term contract supporting laboratory, Fibroscanning and clinical assistance activities.
The role contributes to high-quality clinical research delivery according to agreed targets.
Key Skills for This Role
Full Job Posting
Role overview
Join Panthera Biopartners as a Clinical Trial Assistant at its Preston clinical research site.
This is a 12-month fixed-term contract supporting laboratory, Fibroscanning and clinical assistance activities.
The role contributes to high-quality clinical research delivery according to agreed targets.
Salary and benefits
- The advertised salary is £28,199.
- Benefits include 25 days of annual leave plus bank holidays, with increases based on length of service.
- Additional benefits include life insurance, a healthcare cash plan, family-friendly policies, a cycle-to-work scheme and an electric vehicle scheme.
Key responsibilities
- Process blood, urine and other samples according to study protocols.
- Take blood samples from study participants.
- Coordinate sample transfers with external laboratory vendors and sponsors in accordance with IATA guidelines.
- Operate Fibroscanning equipment on patients within competency frameworks.
- Collect complex data in accordance with Good Clinical Practice.
- Manage emails and phone calls with the site team.
- Assist with preparation for clinical visits.
Skills and capabilities
- A degree in life sciences or a health-related field is required.
- Laboratory experience and excellent clinical skills are required.
- Experience processing complex information and performing data entry is required.
- Excellent attention to detail, a proactive mindset and motivation to learn new skills are required.
About Panthera Biopartners
Panthera Biopartners is an independent Site Management Organisation supporting pharmaceutical and contract research organisations.
The organisation focuses on helping customers find appropriate participants for clinical trials and places patients at the centre of its work.
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