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ISPIN AG

ISPIN AG is a leading Swiss provider of solutions and consulting services related to information security. ISPIN's services all pursue one goal: "Never let cyber threats harm our customers' business!". Our customers should be able to increase their resistance to cyber attacks and at the same time their profitability by using adequate security solutions. As a specialist in IT and information security, ISPIN has excellent know-how and offers a wide range of solutions and specialist expertise. ISPIN finds an individually tailored solution for each customer, consisting of an integral combination of technical, personnel and organizational measures. We are convinced that the future is digital. Digitization will change the way we work, consume and communicate fundamentally change. Things communicate with things, data is more important than goods, startups are revolutionizing industries. The world is being ruled by cyber space and cyber security is becoming a matter of survival. We are convinced that companies and organizations will only survive if they gain the ability to survive in this uncertain digital world.
06/01/2023
Full time
Clinical Data Manager (m/f/d)
ISPIN AG 4051 Basel, BS, Switzerland
Clinical Data Manager The Role: The Clinical Data Manager role is responsible for all aspects of the clinical trial data management process from study start up through database lock and support of clinical study report (CSR) activities for assigned studies. This role may be expected to lead multiple clinical studies. Responsibilities: Serve as lead CDM on assigned clinical trials by attending internal and external clinical trial project team meetings. Responsible for the study-specific data management tasks from protocol review to database lock to ensure data are collected, reviewed, and delivered with high quality, ontime, and within scope. Responsible for the accurate development of CRFs and edit specification per protocol and the completeness of user acceptance testing of CRFs and associated edit specifications for assigned clinical trials. Provide ad-hoc report development, and support database lock and archiving activities. Review and...