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Her expertise spans a diverse range of responsibilities, including: Managed all aspects of clinical studies, provided expert medical monitoring, and oversaw projects to ensure compliance with regulatory standards. Offering valuable medical consultation externally to investigators, sponsors, clients, and internally, acting as the medical representative within project teams. Review adverse events (AEs) and safety reports, ensure accurate coding of AEs and concomitant medications, and prepare reports for submission to regulatory authorities such as the FDA. Playing a pivotal role in meetings with health authorities to address various regulatory activities, leveraging her extensive knowledge and experience. I assist in clinical protocol development, contribute to scientific publications, and provide protocol training both internally for project teams and externally for participating clinical trial sites. Organizing and facilitating various study meetings, investigator meetings, and advisory boards, demonstrating strong leadership and organizational skills. Serving as the internal medical expert for the Board of Directors and potential business partners, offering strategic insights and guidance. Demonstrating proficiency in Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and company standard operating procedures (SOPs). Possesses extensive experience in electronic data capture systems and study-related database software, ensuring efficient data management throughout the research process. Exhibiting broad expertise across multiple therapeutic areas, including Oncology/Hematology, Gastrointestinal (GIT) disorders, Genetic Diseases, Psychiatry, Neurology, Endocrinology, and Infection Control. Iman's wealth of experience and a solid commitment to excellence and innovation make her an asset in pharmaceutical medicine and clinical research.