Looking for experienced Clinical Data Managers to join a leading global full-service CRO. They we're originally a statistical and data management centre of excellence, and now have build upon this to provide a broad range of expertise-based services to worldwide pharmaceutical, biotechnology, and medical device industries and working with some of the most advanced drugs, biologics, and medical devices in development.



Roles: Clinical Data Managers - Multiple vacancies from Junior to Principal



Responsibilities:

Plan, manage, control, and perform data processing and management activities for assigned projects.
Lead assigned data processing and management projects by applying project management skills, data processing, and management techniques.
Specify database validation checks for assigned studies. Lead efforts in developing and maintaining standard database validation checks for common modules as well as for therapeutic/drug area specific modules.
Define and monitor clinical trial dataflow and quality control (QC) processes in accordance to corporate Standard Operating Procedures (SOPs), Good Working Practices, and unit guidelines.
Design and review patient Case Report Forms (CRFs) and database schema. Test data capture/entry screens.


Requirements:

BSc/ MSc in health and/or pharmaceutical sciences, physical/biological, or chemistry fields
Minimum of 2 years experience in clinical trial data capture and management