Director Biostatistics

You are an experienced Associate Director - Biostatistics who will be joining a leading client in the pharmaceutical industry. Your role will be crucial in clinical development, involving tasks such as contributing to trial design, analysis planning, interpretation of results, and regulatory submissions. Your key responsibilities will include collaborating on innovative and efficient clinical trial designs to ensure alignment with study objectives. You will independently author and review protocols, statistical analysis plans, and clinical study reports. Providing statistical leadership in regulatory interactions, publications, and presentations will also be part of your role. Additionally, you will manage multiple studies to ensure consistency and adherence to industry standards. Your expertise in statistical methodologies and clinical trial design will be applied within a dynamic development environment. You will act as a strategic partner in cross-functional teams, contributing to drug development strategies. It is essential to maintain compliance with processes, SOPs, and global project standards. Furthermore, you will have the opportunity to mentor and develop team members while fostering a collaborative and inclusive culture. The ideal candidate for this role should have extensive experience in biostatistics within clinical development. Strong knowledge of statistical methods and regulatory requirements is required. You should also possess the ability to communicate complex statistical concepts to cross-functional teams and demonstrate proven leadership skills with a collaborative mindset. This is an exciting opportunity to work with a leading pharmaceutical company in an innovative and data-driven environment. If you are passionate about biostatistics and eager to make a meaningful impact, we encourage you to connect with us! Feel free to reach out for more details or apply today.,