Cytel is seeking a Principal Biostatistician to provide statistical leadership for our pharma client projects, leading late‑phase (II/III) drug development and regulatory submissions, with a focus on Gastrointestinal studies.
You will lead statistical teams, influence study designs and analysis plans, review reports for submissions, and collaborate with cross‑functional sponsor teams. A Ph.D. is preferred and extensive SAS/R expertise is required.
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Principal Biostatistician - Lead Late-Phase Trials 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.
