Cytel is seeking a Senior Biostatistician to support or lead Phase I–IV clinical studies, embedded with a pharmaceutical client. You will provide statistical leadership, develop SAPs, design studies, and ensure regulatory submissions meet CDISC and FDA guidelines.
Ideal candidates bring 5+ years of trial experience, SAS and R programming skills, and a strong ability to communicate complex statistics to non-statisticians. Collaboration across CROs and internal teams is essential.
Senior Biostatistician - Clinical Trials Lead (Phase I-IV) employer: Cytel
Cytel is an exceptional employer that empowers its employees to thrive in a collaborative and innovative environment, particularly for the role of Principal SAS Programmer. With a strong commitment to professional development and training, Cytel ensures that you have the support needed to excel in your career while working remotely with a leading global pharmaceutical client. The company values diversity of thought and encourages autonomy, making it an ideal place for those looking to make a meaningful impact in the field of clinical trials.
