
Dr. Mohammed Abdul Maleque Molla
Member
Biography
Dr. Mohammed Abdul Maleque Molla is a distinguished pediatrician with extensive qualifications, including DCH, MRCP (UK), MRCPCH (UK), FRCP (Ed), and FRCPCH (London). He is a Clinical Assistant Professor in Pediatrics at multiple universities in Riyadh, Saudi Arabia, and a Consultant Pediatrician & Pediatric Intensivist at Al Yamamah Hospital. Dr. Molla has vast experience in neonatology, pediatric pulmonology, and intensive care.
His professional journey spans various prestigious roles, including consultant pediatric intensivist and neonatologist, and registrar positions in pediatric medicine. He has been involved in training postgraduate students and is a member of multiple professional associations like the Saudi Pediatric Association and the European Society of Critical Care.
Dr. Molla has contributed significantly to research, with several publications in renowned journals such as Annals of Saudi Medicine and The Lancet. His research focuses on pediatric conditions like infantile hypophosphatasia, congenital eventration of the diaphragm, and X-linked hypophosphatemic rickets. He has also participated in various administrative and leadership roles, including as the program director for the Saudi pediatric board and coordinator for the WHO Polio Eradication Program in Riyadh.
Dr. Molla’s expertise in pediatric care, teaching, and research makes him a valuable contributor to medical education and healthcare.
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.