Hasan Abbas, M.D

Fellowship-trained physician (MD, India) with over 15 years of combined clinical and research experience as a Vitreoretinal Surgeon. Strong knowledge of clinical trial design, methodology, and regulatory compliance, with a meticulous approach to evaluating and communicating scientific and clinical data. Seeking an opportunity transitioning into a Medical Science Liaison (MSL) role, bringing a robust foundation in clinical science, evidence-based medicine, and scientific communication - Currently engaged in Early phase I/II oncology Clinical trails as a Clinical Research Coordinator, Clinical research and Publications. Coordinate Phase 1/II and early-phase oncology clinical trials, ensuring compliance with regulatory requirements and adherence to study protocols. •Identify, screen, and compile lists of potential research subjects aligned with study objectives tooptimize recruitment efforts, including obtaining informed consent and ensuring adherence toinclusion and exclusion criteria. •Conduct and document face-to-face and telephone interviews with study subjects, adhering toestablished data collection protocols and documentation standards. •Collaborate with study sponsors, principal investigators, and study staff to develop and revisestudy documents, including protocols and informed consent forms, ensuring clarity andregulatory compliance. •Enter data into Electronic Data Capture (EDC) systems, including Medidata and REDCap, andmonitor data collection processes to ensure accuracy and compliance with Good Clinical Practice(GCP) and institutional policies. •File and address protocol deviations with sponsors and the Institutional Review Board (IRB), aswell as report Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs) tosponsors. •Schedule monitoring visits and respond to queries to ensure site performance, data accuracy, andregulatory compliance across multiple clinical trials. •Review and evaluate study-related documents to confirm adherence to GCP and FDA regulations. •Oversee the planning, implementation, and management of clinical trials in accordance with regulatory guidelines and study protocols. •Conduct training sessions for study staff on protocol requirements and documentation practices toensure consistent implementation and compliance. •Write and contribute to scholarly publications, enhancing the dissemination of research findings and insights within the scientific community.