Professional Experience in Clinical Research
Collaborative Research Environment
I have specialised in fostering collaborative environments that effectively bridge academia and industry. My experience encompasses working alongside diverse teams to secure research funding, successfully applying for grants, and facilitating the professional development of research staff. I have also been involved in establishing research partnerships and joint ventures, contributing to dynamic and productive research collaborations.
Ethical Aspects and Regulatory Knowledge
My expertise includes a thorough understanding of the ethical considerations essential for the conduct of clinical trials. I am well-versed in training research staff, managing clinical procedures, designing trials, developing study protocols, preparing regulatory submissions, recruiting subjects, obtaining informed consent, and maintaining comprehensive documentation. I have actively participated in the planning and management of clinical studies, ensuring all ethical and regulatory requirements are met.
Critical Review and Analysis
As a critical thinker, I am deeply interested in the critical review and analysis of research journals, particularly regarding their assessment methods, external validity, reliability, and statistical power. I have gained valuable experience through participation in journal clubs, focusing on critical analysis and appraisal of scientific literature.
Public Health Research and Ethics Committee Representation
I am familiar with the use of analytical tools in public health research and epidemiology. For two years, I represented the Clinical Research Centre on the Ethics Committee, which provided me with a comprehensive understanding of the various ethical concerns involved in clinical trials. The centre was engaged in more than fifty clinical trials across a range of therapeutic areas, including device trials.