
Dr. Md. Sibly Sadik Shuvo
Member
Biography
Dr. Md. Sibly Sadik Shuvo is a dedicated medical professional with an MBBS, CCD, and MPH. He has extensive experience in clinical research and healthcare, particularly in cardiology and public health. Dr. Shuvo has worked with several prestigious institutions, including the National Heart Foundation & Research Institute, NIPSOM, and AMZ Hospital, where he served as a Research Medical Officer, Data Enumerator, and Senior Medical Officer. His research includes projects on hypertension, tobacco consumption, and the health workforce during the COVID-19 pandemic.
Dr. Shuvo's work spans multiple roles in patient management, clinical governance, and data analysis, where he coordinated medical activities, supervised patient care, and organized training sessions for healthcare staff. He is skilled in data analytics, policy development, and program planning, with proficiency in SPSS, MS Office, and Internet browsing. Dr. Shuvo is also committed to improving healthcare through patient education and collaboration with multidisciplinary teams. Fluent in both Bengali and English, he has a strong foundation in leadership, community partnership, and public health sciences.
Dr. Shuvo aims to continue his professional development while contributing to healthcare improvement in Bangladesh. He is married and resides in Dhaka.
Job Responsibilities
- Ensure research adheres to ethical guidelines such as the Declaration of Helsinki and Good Clinical Practice (GCP).
- Assess study protocols, informed consent forms, and investigator qualifications.
- Verify informed consent documents are clear, comprehensive, and compliant.
- Oversee study progress, review adverse events, and ensure protocol adherence.
- Ensure compliance with regulatory laws and guidelines, such as FDA and EMA standards.
- Maintain impartiality by avoiding conflicts of interest and preserving confidentiality.
- Keep accurate documentation of IRB decisions, meeting minutes, and communications.
- Act as a liaison between sponsors, investigators, and regulatory authorities.
- Stay updated on regulatory developments and contribute to ethical training programs.