Mohammed Seedat

Background

About Mohammed Seedat

I am a dedicated and passionate Clinical Research professional with over 3 years of hands-on experience in managing and coordinating clinical trials, including in diverse therapeutic areas such infectious diseases, reproductive health, PK studies and medical devices. My mission is to contribute to the advancement of healthcare through safe, ethical, and efficient clinical trials. With a track record of leading over 20 trials, I thrive on fostering collaboration with multidisciplinary teams, ensuring quality monitoring, and consistently meeting tight deadlines and budgets. I have a proven ability to train and mentor clinical staff, and I pride myself on my attention to detail and ability to execute under pressure. As a top 30 under 30 youth leader recognized for my contributions to clinical research, I am committed to using my knowledge to further improve clinical trial processes and patient safety. Whether managing investigational products, ensuring zero protocol deviations, or leading internal quality assurance initiatives, I’m always focused on delivering results that matter. I’m looking forward to connecting with others in the clinical research community to exchange insights and continue growing in this ever-evolving field! Key Skills: Expertise in clinical trial management (Phase I-IV) Investigational product management & regulatory compliance ICH-GCP and local regulatory requirements (SAPC, SAHPRA) Data management & EDC systems (Medidata, RAVE, Redcap) Team leadership & training Quality assurance and continuous process improvement Feel free to reach out if you’d like to connect or discuss clinical research trends!