Medically qualified with extensive experience in drug development. Strong track record in preclinical study and medical research in both academic and industry environments. Expert in project development, data analysis, ethical application, and regulation compliance. Ability to ensure the successful execution of projects, report progress, and prepare publications. Experienced in liaising effectively with research partners, sponsors, and regulatory authorities. Knowledge in designing and interpreting clinical trials. Seeking a challenging position to contribute to advancements in medical research.