When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. As an experienced Biostatistician, you will lead research design and analytical strategies, provide input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts. You will use your knowledge to advise, provide guidance and to oversee the quality control of statistical deliverables. As the functional lead within a study team, you will direct the Biostatistical activities on a study and be accountable for the deliverables. Senior, Principal, and Senior Principle level Biostatisticians at Parexel are client-facing and play an integral part in the study team. Our Biostatistics teams are not only focused on delivering quality results for our client’s needs, but also value working with one another in a flexible environment. Although some team members are home-based and others are office-based, our virtual resources support our teams to work collaboratively and effectively across the globe. Our Biostatisticians are not only focused on delivering quality results for our client’s needs, but also value working with one another. Our virtual resources support our teams to work collaboratively and effectively across the globe. The overall long tenure of our team integrates a depth of knowledge and experience. Working together, you will create paths to answers and contribute to new therapies which ultimately will impact the patient. What you’ll do Supervise, advise and review: Leverage your expertise. Develop complex analysis strategies and execute them using efficient programming techniques (software: SAS, R). Foster teamwork. Perform intricate statistical analyses and provide input to statistical reports. Share knowledge. Provide input to analysis plans, statistical reports, statistical sections of integrated clinical reports. Impact the process. Be a proactive advisor for all types of analysis from the proposal process through the project life cycle. Take quality seriously. Review analysis data sets and quality control all types of statistical analysis deliverables. Coach and mentor. Train and uplift junior members of the department. Cooperate and network: Build relationships. Liaise with other biostatistical and company departments to optimize global efficiency. Work collaboratively. Coordinate Biostatistics related project activities for successful completion within given timelines and budget. Interact with heart. Coordinate with clients with regard to data analysis, scope of work, and budget. Demonstrate our expertise. Represent Parexel at client meetings. More about you On your first day we’ll expect you to have: Experience: A minimum of 5 years industry (or directly relevant) experience with an M.Sc., or a PhD plus 2 years of industry experience A thorough understanding of the statistical aspects of clinical trials Experience in statistical analysis in a clinically related subject, either within clinical trials or in Epidemiology SAS programming or R programming skills Education: A Masters or Ph.D. level education in biostatistics, statistics, mathematics, or another relevant discipline Skills: Confidence, be self-reliant and a quick learner who enjoys working in a matrixed team Good leadership skills Strong oral and written English communication skills The ability to travel as required, although this is not frequent A strong work ethic to promote the development of life changing treatments for patients Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.