Junior Clinical Data Manager

Job content

• You will be responsible for the development and implementation of clinical data studies
• You will support the management all activities covering the data management process including set-up, remote monitoring and data base lock
• You will provide clinical data management support to clinical projects
• You will review and update clinical study documents (e.g. protocols)
• You will set up the clinical database including consistency checks defined in the Data Validation Plan
• You will coordinate the clinical data quality review during the study execution
• You will collaborate with Biostatisticians on data validation and lock of the database, including management of discrepancies
• You will prepare and maintain key documents for the data management
• You will collaborate with cross-functional internal resources (clinical project manager, scientists, medical directors) on different health benefit areas
  

• MSc degree with a scientific background
• At least 1 or 2 years’ experience in the field of clinical research
• Up to date on regulations regarding clinical data collection and on clinical data standards such as: GCP (Good Clinical Practice), GCDMP (Good Clinical Data Management Practices), data privacy, and new regulations like GDPR (General Data Protection Regulation)
• Experience with Medidata is a must
• Project management skills
• Central monitoring and analytical skills are a plus
• Problem solving skills with a desire to improve current processes
• Ability to ‘think outside of the box’
• Excellent communication skills, both oral and written in English