Clinical Data Manager (m/f)

- Coordinate and perform Clinical Data Management (CDM) activities for assigned studies
- Review all documents for assigned studies
- Write Data Management Plans (DMPs)
- Perform Data Validation and Cleaning plans
- Define and Specify data requirements (CRFs) and validation for assigned studies
- Program reports supporting clinical data cleaning
- Ensure that study timelines are met
- Perform User Acceptance Testing of databases
- Perform User Acceptance Testing on validation checks
- Track data flow and review status and provide updates to team
- Assist with development of Case Report Forms (eCRFs)
- Participate in development and review of policies, SOPs and associated documents for CDM
- Review data according to DMP, SOPs and associated documents

- Profound experience (including experience in managing study level projects in medical device, medical research or pharmaceutical industry)
- Knowledge and experience in Medidata Rave suite (i.e. EDC, query management, reporting system and architect) and other data management tools
- Bachelor degree in computer science or related discipline (e.g. biostatistics)
- Excellent written and verbal communication skills, analytical skills, strong organizational skills, self-motivated, flexibility and adaptability
- Ability to work independently in a cross-functional team environment

Weitere Qualifikationen: Clinical data manager