Cytel is seeking a Senior Clinical Data Manager to provide comprehensive data management support for assigned clinical studies. You will perform ongoing data review to ensure accuracy, completeness, and consistency with the protocol and data management plan.
A minimum of four years in clinical data management and hands-on data review experience is required. Expertise in Medidata Rave is preferred, with a strong understanding of CDM processes and regulatory requirements (GCP, FDA, ICH).
Senior Clinical Data Manager: Medidata Rave Expert 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.
