ABDOULIE GIBBA, Clinical Trial Application/ HND Computer ScienceClinical Trial Application DeveloperProfileResearchProfileA highly skilled Clinical Trial Application Developer with 5 years of experience in designing, developing, and maintaining clinical trial software and electronic data capture (EDC) systems. Expertise in translating clinical study protocols into functional applications, ensuring compliance with regulatory standards such as GCP, FDA, and ICH guidelines. Proficient in various programming languages and database management systems, with a strong background in healthcare and clinical research environments. Key Skills: Programming Languages: Python, Databases: SQL, open clinica Web Technologies: HTML, CSS Regulatory Compliance: Good Clinical Practice (GCP), FDA 21 CFR Part 11, ICH Guidelines Data Security: HIPAA compliance, data encryption, secure access controls Communication & Collaboration: Excellent verbal and written communication skills, experience working with cross-functional teams including clinical, regulatory, and IT staff As a seasoned data-driven professional since 2012, I began my career as a Data Entry Clerk and later became a Data Manager at the Medical Research Council The Gambia @ London School of Hygiene and Tropical Medicine. In this role, I managed data supervisors and data entry clerks. Currently, I am a Clinical Trial Application Developer (REDCap) at Queen Mary University of London. I have extensive experience working in a medical research setting, managing research studies (including clinical trials, vaccine trials, device trials, and observational studies) and systems using software such as REDCap, OpenClinica, SQL, and more. I have led multi-center and multi-site research studies across different countries, taking the lead as a Data Manager and utilizing various tools to execute data management tasks. I am highly skilled in data governance and have significantly contributed to developing standard operating procedures (SOPs) for our data management department. I have also gained experience and training in General Data Protection Regulation (GDPR), Good Clinical Practice (GCP), research ethics, 21 CFR Part 11 regulation, and HIPAA compliance.ResearchResearch Interests: As a database developer, I have a strong interest in ensuring the development of a proper and robust database system that stores research data with high quality and good performance. My focus includes optimization and efficient data retrieval to enable quality analysis and produce better results. Additionally, I have a keen interest in abstract writing