The Nonclinical Regulatory Management Lead at Astellas Pharmaceutical is responsible for overseeing regulatory submissions and ensuring compliance with nonclinical data requirements. Candidates should have a strong background in regulatory affairs, particularly in nonclinical studies, and experience in managing regulatory submissions. The role requires excellent communication skills, attention to detail, and the ability to work collaboratively with cross-functional teams. A deep understanding of global regulatory guidelines and the ability to strategize regulatory pathways are essential.
Astellas Pharmaceutical is a global pharmaceutical company headquartered in Tokyo, Japan. It focuses on improving the health of people around the world through innovative and reliable pharmaceutical products. Astellas is committed to addressing unmet medical needs and enhancing the quality of life for patients. The company operates in various therapeutic areas, including oncology, urology, immunology, and neuroscience. With a strong emphasis on research and development, Astellas aims to bring new and effective treatments to market, leveraging its expertise in biotechnology and advanced drug discovery.
Japan is a vibrant country with a rich cultural heritage and a high standard of living. Job opportunities are abundant, especially in the technology, healthcare, and engineering sectors. The work culture is known for its discipline and dedication. Japan offers a unique blend of traditional and modern lifestyles, with bustling cities and serene countryside. The cost of living can be high, particularly in urban areas. For those relocating, Japan has a straightforward visa process for skilled workers, but learning Japanese is beneficial. The country is renowned for its efficient public transport, safety, and excellent healthcare system, making it an attractive destination for expatriates.
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