Clinical Trials Officer - Bristol, United Kingdom - North Bristol NHS Trust

Tom O´Connor

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Tom O´Connor

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Description

Please review the job descrition for more detailed information regarding main responsibilities: Ares of key responsibilities relate to the following areas: Clinical trial set up and running Reviewing research proposals and associated study documentation, appraise risk and undertake sposnorship review on behalf of NBT.

Working with stakeholders to ensure all governance and regulatory checks have been carried out prior to R&D approvals. Overseeing study delivery and ensure research compliance and reporting is adhered to Performance management. Oversee performance of NBT sponsored studeies working with stakeholders to identify and address poor recruitment.


Be responsible for fulfulling the trust monitoring obligations in line with the Reesarch Governance Framework and Clinica Trials Regulations To be responsible for identifying corrective and preventative action and ensuring this is implemented to address the findings of study monitoring activities.

Compile safety monitoring data for MHRA, regulatory authorities, the Trust board and for R&D internal review Other Accountable for own actions in accordance with appropriate Code of Professional Conduct, Trust policies and procedures Maintain responsibility for own professional and specialist development Responsible for the quality of data maintained within R&D pertaining to studies registered on the R&D IT system, currently EDGE Assist Research Compliance Manager in developing, implementing, and maintaining a networked approach as a local response to national developments in Research and Development

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