Hybrid Senior Clinical Data Associate | Data Management

Cti; Lisboa; Hybrid; EUR 45,000 - 65,000; Full time

Job summary

CTI Clinical Trial and Consulting Services in Portugal is seeking an experienced Clinical Data Manager to support data management activities across clinical studies in a GMP-compliant environment. You will review CRFs, ensure data quality, and maintain essential study documentation.

The role involves training CDA staff, refining SOPs, and coordinating with management to implement efficient data workflows under GCP/ICH guidelines. Hybrid work options may be available in this role.

Qualifications

• Experience in data management for clinical studies.
• Knowledge of GMP/GCP/ICH guidelines.
• Familiarity with CRF workflows and SDTM is a plus.

Responsibilities

• Review CRFs for data quality and consistency.
• Maintain essential study documentation and data locks.
• Coordinate with management to implement efficient data workflows.
• Train CDA staff and refine SOPs.

Skills

Data management

GCP/ICH guidelines

CRF review

SOP development

Training

Job description

CTI Clinical Trial and Consulting Services in Portugal is seeking an experienced Clinical Data Manager to support data management activities across clinical studies in a GMP-compliant environment. You will review CRFs, ensure data quality, and maintain essential study documentation.

The role involves training CDA staff, refining SOPs, and coordinating with management to implement efficient data workflows under GCP/ICH guidelines. Hybrid work options may be available in this role.