Tom H. Email and Phone Number

Coordinating CTIMPs/non-CTIMPs within the Genomic Medicine research team focusing on Metabolic research. Ensuring that comprehensive, high quality and efficient processes are in place for setting up studies, organising necessary approvals, data management, managing external staff visits, ensuring full compliance with the regulatory framework; including financial management of study set-up costs and income recovery for Genomic Medicine. Working with CROs to ensure commercial studies are fully monitored and data queries are resolved. Research studies worked on include; recent SAR-CoV-2 vaccines trials, Metabolic enzyme replacement therapy trials and numerous genetic/metabolic non-CTIMPs.

Data management for natural history studies and follow-on CTIMP registries specialising in Genomic Medicine - Metabolic Disorders. Coordination of a diagnostic study by organising patient study visits, consenting participants and submitting APR & Ethics amendments. SARS-CoV-2 study experience working on ENSEMBLE2 and ISARIC throughout the 2020-21 pandemic.

Collecting relevant patient information pertaining to personal and legal requests for medical patient records in adherence to data protection laws. Liaising with solicitors, police, other health trusts and government to complete requests within compliance timeframes.

Preparing relevant patient records, such as radiology images & histology, for cancer pathways multidisciplinary team meetings. Recording data & MDT outcomes whilst tracking patient pathways.

Collecting, storing & archiving medical records