Senior Clinical Data Manager - Hybrid, Impacting Treatments

CTI; Lisboa; Híbrido; EUR 42 000 - 66 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Hybrid work from home opportunities

Health benefits

Vacation package

CTI Cares program

Resumo da oferta

CTI in Portugal is seeking a Clinical Data Management (CDM) lead to act as the primary CDM contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific CDM document development and maintenance, project status reports to the CTI project team, and data cleaning from start-up through archival.

You will coordinate data receipt from external sources, develop and approve project database builds, test and validate, and ensure GSOP compliance while maintaining

Qualificações

• 2 years of related Clinical Data Management experience.
• Bachelor’s degree in nursing or life science is required or an equivalent combination of education and clinical research experience.

Responsabilidades

• Perform and/or direct CDM team activities to meet project deliverables on schedule and within budget.
• Develop and maintain study-specific documents (CRFs, guidelines, CDMP, annotated CRFs, edit specs).
• Represent CTI CDM on project teams and communicate progress to sponsors.
• Maintain relationships with internal customers and Sponsors, updating plans as needed.
• Coordinate data receipt from external sources and ensure timely processing.
• Monitor CDM team quality and compliance with GSOPs; provide feedback.
• Prepare project reports for sponsors, project teams, and CTI management.

Conhecimentos

CDM experience

Project coordination

Formação académica

Bachelor’s degree in nursing or life science

Descrição da oferta de emprego

CTI in Portugal is seeking a Clinical Data Management (CDM) lead to act as the primary CDM contact with sponsors and represent the DM group on CTI project teams. Responsible for study-specific CDM document development and maintenance, project status reports to the CTI project team, and data cleaning from start-up through archival.

You will coordinate data receipt from external sources, develop and approve project database builds, test and validate, and ensure GSOP compliance while maintaining