Cytel is seeking a Senior Biostatistician to support or lead clinical studies from design through submission. You will perform ad-hoc and regulatory-relevant analyses, collaborate with clients and CROs, and contribute to SAPs, CSRs and data standards.
You will have a strong statistical background, experience with CDISC/ADaM, and excellent communication to explain methodology. This role is embedded with a pharmaceutical client and requires proactive leadership.
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Senior Biostatistician: Clinical Trials & Submissions Lead 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.
