Daniel Chung Email & Phone Number

Mitcham, Gb

London Area, United Kingdom

London, England, United Kingdom

 Leading the clinical site department on all aspects of clinical trial conduct, focusing on clinical trial set-up to close-out of site related matters in accordance with protocol requirements for operational implementation to provide the best product for both CTIMP and non-CTIMP trials.  First point of contact for internal stakeholders, acting as cross-functional liaise between project management to the rest of the department functional leads e.g. Clinical Coordinators, Pharmacists, Laboratory Leads, Data Leads etc. to ensure effective communication throughout. Key study team member in internal/external meetings with clients to communicate site considerations and updates. Developing detailed schedule of activities and implementation into operational use. Maintenance of Trial Master/Investigator Site files and participating in both internal/external audits. Managing training and overseeing clinical site staff ensuring appropriate resources are in place and that all staff are trained to conduct the study to the required quality standards. Direct communication with CRAs to identify monitoring deviation trends, completing root cause analysis, CAPA investigations, and provide novel solutions to reduce incident rate.  Cross-functional support, management of IMP documentation/processes e.g, pharmacy manuals, site blinding plans, accountability forms, administration forms, notification of dose, and liaising with vendors to organise the logistics of IMP receipt/destruction. Writing SOPs, guidelines and creating tools, to ensure that the department works within quality systems and meets all regulatory requirements and principles of GCP.

London, England, United Kingdom

 Coordinated delivery and ongoing management of Phase I-III clinical trials, including First-in-Human trials and Japanese bridging studies, which encompassed clinical trial set-ups, submission documents, substantial & non-substantial amendment reviews of protocols, green-light signoffs, master treatment schedule set-ups, study operation manual drafting & amendments, and other clinical trial related documentation. Point of contact for internal/external stakeholders for study specific queries i.e. Sponsors, R&D, Principal Investigator’s, and medical research team. Scheduled and responded to monitor requests and action items. Completed root cause analysis, and actioning of CAPAs. Performed clinical assessments from screening of clinical trial participants to the completion of study duration of each cohort, e.g. ECG, Vital signs, Orthostatic Vital signs, Phlebotomy, Spirometry, and, Dosing related procedures etc. Robust knowledge in different types of dosing procedures and processes e.g. via intravenous line (IV), site injection, capsules, fluids etc. Provided effective day-to-day onsite management to ensure timely execution of study related assessments, reducing query incident rate by 30% across multiple active studies. Scheduled and led safety review committee meetings to evaluate volunteer safety and adapted changes to dosing regimens in response to decisions made to dose escalation/de-escalation.

Sittingbourne, England, United Kingdom

ALS is a leading global provider of food and drink testing. I was given an opportunity to work as a laboratory technician at one of their six accredited laboratories in the UK. Leading a team of laboratory technicians on aspects of microbial cultivation and sample processing of food products for external stakeholders. Gained and maintained strong knowledge relating to the field of microbiology e.g culturing techniques, identification procedures, and assay processes. Conducted laboratory risk assessments and implemented organisational improvements to enable risk mitigation and increased rate of sample analysis.

Immunology Msc, Immunology, Merit

MSc Project Title: Analysis of New Novel Type 3 Dendritic Cells in Breast Cancer I worked within a small team to further characterise.

Biomedical Science Bsc Hons, Life Sciences, 2:1

Bsc Project Title: The Effects of Different Dietary Fibres on The Growth of Gut Microorganisms During my research, I was successful.