Senior Clinical Data Associate Drive Data Quality in Trials

ThermoFisher Scientific; Buenos Aires; Sur place; ARS 57 911 000 - 70 103 000; Plein temps

Résumé du poste

Thermo Fisher Scientific in Buenos Aires, Argentina is seeking a Senior Clinical Data Associate to ensure clinical data quality and integrity across trials. You will perform data cleaning with minimal supervision, adhering to GCP and SOPs, and support data validation activities to assess safety and efficacy of investigational products.

The role involves setting up study activities, reviewing data listings, and acting as SME for study-specific processes.

Qualifications

• Bachelor's degree or equivalent in a life sciences field.
• 0-2 years of relevant clinical data management experience.
• Equivalency considered with education, training, or related experience.

Responsabilités

• Supports the setup of study activities such as database design, testing of data entry screens, and Data Validation Manual (DVM) creation, as required.
• Reviews data listings for accuracy and consistency of data.
• Acts as point person and subject matter expert for specialized study-specific processes.
• Generates, tracks and resolves data clarifications and queries and makes changes to the clinical database as required.
• Contributes to the improvement of data management processes on a global level.
• Produces project-specific status reports for management and/or clients on a regular basis.
• Provides training and work direction to junior staff as required.

Connaissances

Attention to detail

Written and verbal communication

Analytical/problem-solving

Regulatory compliance

Data management

Confidentiality handling

Formation

Bachelor's degree or equivalent in a life sciences field

Description du poste

Thermo Fisher Scientific in Buenos Aires, Argentina is seeking a Senior Clinical Data Associate to ensure clinical data quality and integrity across trials. You will perform data cleaning with minimal supervision, adhering to GCP and SOPs, and support data validation activities to assess safety and efficacy of investigational products.

The role involves setting up study activities, reviewing data listings, and acting as SME for study-specific processes.