CRF Laboratory Technician

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Main Duties and Responsibilities 
 Be responsible for the management of samples received and stored at the CRF 
 Be responsible for the maintenance of the storage facilities and ensure that temperatures 
are maintained within set limits. 
Respond to alarms when necessary during working hours to ensure storage facilities are 
maintained within set limits 
To be able to follow departmental SOPs and prepare samples accurately 
To be able to use computer systems correctly, enter data accurately from transcription 
sheets or request forms  
To assist in the training and supervision of staff working in the CRF as part of their 
induction. 
To support the Quality Assurance Manager in the development of the CRF tracked Sample 
Storage Facility 
To attend and contribute to any meetings and SIV’s in relation to Clinical Trials and sample 
management and to feedback and recommend any changes and/or improvements to the 
service as appropriate to the CRF Team Leader or Principal Investigator 
To be responsible for the implementation of SOP’s and procedures specific to Clinical Trial 
Protocols that will have an impact within the CRF department 
To contribute to wider policies that have an impact within the CRF and across the Trust 
To assist in the regular review and update of SOP’s and procedures as agreed with the 
QA Manager. 
To propose changes to working practices and Sample preparation techniques that will 
maximise the potential for efficiency and safety 
To be knowledgeable on the current framework of ICH-GCP guidance, MHRA and HTA 
legislation and Research Governance. 
To ensure that both commercial and non-commercial trials are managed and maintained 
within the framework of current ICH-GCP guidance, MHRA and HTA legislation and 
Research Governance 
Actively participate in the development and management of PBMC preparation service. 
 Working closely with CRF Pharmacy technician in continuous maintenance and servicing 
of CRF’s laminar flow cabinet 
 To participate in implementing a potential sample management system at the CRF 
 Actively engage in the EEG (electroencephalogram) working group and any development 
activities  

Patient/Client Care 
To deliver a customer-focused service and to adhere to the highest principles of customer 
service when dealing with Sponsors, staff and the public. 
Promote Good Laboratory Practice. 
Be able to check and prepare samples according to standard and study protocols 
To provide support to external stakeholders during monitoring visits  

Financial/Resource Management  
Be responsible for the stock control and for the return and subsequent storage and 
reconciliation or disposal of Clinical Trials stock 
Be responsible for the stock control subsequent storage and reconciliation of consumables  
related to the management of CRF samples 
To immediately report any deficiency in equipment and systems to the QA Manager and 
escalate as needed 
Ensure consumables used within CRF are purchased, stored, and used within safe 
systems 
Ensure consumables purchased or received are used within date to ensure cost 
effectiveness 
Advise external departments of costs related to the collection and storage of samples