Senior Statistician for Clinical Development

The position

As a Statistician for Clinical Development with a senior profile your responsibilities will include: Taking charge of representing Biostatistics within cross-functional trial teams, collaborating closely with statistical programmers Leading the evaluation of clinical trial data, meticulously assessing the impact of data quality on statistical analyses, and spearheading sample size calculations Guiding and elucidating statistical requirements and concepts to stakeholders, including medical doctors and trial managers, to ensure a cohesive understanding Orchestrating specified statistical analyses, skillfully interpreting and articulately reporting trial results Championing the preparation of submissions to regulatory authorities, ensuring adherence to rigorous standards and compliance As a Statistician for Clinical Development with a junior profile your responsibilities will include: Assisting in representing Biostatistics within cross-functional trial teams, working closely alongside senior statisticians and statistical programmers. Supporting the evaluation of clinical trial data, aiding in the assessment of data quality's impact on statistical analyses, and contributing to sample size calculations. Providing support in explaining statistical requirements and concepts to stakeholders, collaborating with senior members to ensure effective communication. Contributing to specified statistical analyses, learning from interpretations and reports provided by senior statisticians. Assisting in preparing submissions to regulatory authorities, gaining valuable experience under the guidance of senior colleagues. Qualifications If you are a Senior profile we expect you to have: A strong background in mathematics and statistics corresponding to MSc level. 3+ years of experience as a statistician or a PhD within clinical or biostatistical research. Experience with R, SAS, or other programming languages. For a Junior profile, you have: A strong background in mathematics and statistics corresponding to MSc level or Phd Experience with R, SAS, or other programming languages. It would be a strong advantage if you have experience in: Project management and cross-functional collaboration. Working in a global organization in a highly regulated industry. About the department Our Biostatistics organization consists of people located in Denmark, India, China, Japan, Spain, UK, and the US. We offer a wide variety of statistical tasks and challenges, providing a large scientific community. We strive for an inspiring working environment with a focus on collaboration and opportunities for personal growth and development. Our daily work is characterized by a positive and informal atmosphere, as well as a sustainable balance between work and other priorities. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a -year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63, employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing.