Clinical Data Programmer II

About the role

The core responsibility for this position is as a member of the Data Management department at Novotech. The Clinical Data Programmer-II (CDP-II) will be responsible for programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP).

What you'll do

• The CDP-II shall be responsible for programming activities on a project
• This shall include designing and implementation of clinical database, programming of data review listings and programming of data reconciliation
• The CDP-II shall ensure quality standards per SOPs and ICH-GCP
• Participates in project team meetings as required
• The CDP-II shall be responsible for designing, programming, testing and maintenance of clinical trial databases in different clinical trial applications in accordance…

What you need

• 2–5 yrs of experience
• Clinical research
• SOP writing
• CRO
• Reconciliation
• Clinical data management
• Any graduate