This role is responsible for conducting of testing for clinical research projects and clinical trials. The main duties of the role include:
Routine use of the Laboratory Information Management System (LIMs).
The performance of various analytical procedures including various manual screening and automated methods covering a wide variety of clinical diagnostics tests.
The preparation and handling of samples and diagnostic reagents.
The operation of various automated analytical systems
The accurate maintenance of analytical records.
Strict adherence of chain of custody procedures throughout the analytical process.
The routine maintenance and calibration of analytical instrumentation.
The preparation of specimens for transportation to ensure that their stability is safeguarded during shipment to the appropriate analytical laboratory.
Recording and monitoring of temperature for the laboratory and equipment.
Perform troubleshooting on technical issues.
Ensuring that all the necessary quality control checks are completed daily and that they meet internal criteria.
Participation in quality audits
Preparation of data reports and data checks required for clinical studies
Who can apply?
Qualified to at least bachelors level in a Life Science or Chemistry subject
Excellent communication and organisational skills
Ability to work as a team member of a cross-functional team.
Ability to work under pressure to meet deadlines.
Strong work ethic and self-starter attitude
Strong attention to detail
Bachelors or masters degree in biomedical science.
Previous laboratory experience
Previous experience working on clinical trials
Previous experience in a clinical testing laboratory
Working knowledge of quality systems
Working knowledge of Health and Safety, including CoSHH
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