Cytel invites a Biostatistician to support Phase I–IV clinical studies. You will perform ad-hoc analyses, design discussions, SAS/R analyses, and contribute to regulatory submissions. You will collaborate across clinical, data management, and regulatory teams to drive study success.
A Master’s in statistics is required, and 3+ years in pharma/biotech trials; PhD strongly desired for advanced roles. The position is embedded with a client and located in the UK.
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Embedded Biostatistician: Clinical Trials Leader 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.
