RBM Central Monitor & Data Quality Specialist

Comcap Holdings Llc; Buenos Aires; Hybrid; ARS 1.200.000 - 1.800.000; Vollzeit

Zusammenfassung

Pfizer in Buenos Aires offers a hybrid Senior Associate, Central Monitor role focused on RBM-enabled data surveillance in clinical studies. You will help ensure data integrity and regulatory compliance while supporting global study teams.

The position requires 3-5 years in clinical development, strong data management and technical skills, and the ability to coordinate with stakeholders 2–3 days weekly in-office.

Qualifikationen

• Bachelor’s degree or above of equivalent experience in a scientific or business related discipline required.
• 3 - 5 years working experience in the clinical development fields.
• Working knowledge of clinical development process, understanding concepts of Phase I-IV and principles of study design
• Previous experience within a data management role, understanding key processes and principles associated with role including CRF design, database set-up, edit check specification, DMPs and data cleaning activities
• Knowledge of clinical trial database and its applications
• Knowledge of Windows Environment and its applications (Word, Excel, PowerPoint, Project, etc.)
• Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills.

Aufgaben

• Implement global strategies, initiatives, processes, and standards to ensure consistent, efficient, and quality processes to meet quality, timelines and deliverables.
• Provide technical expertise to set up and test study level Risk-based Monitoring system
• Review study level system outputs to process for the signal and action management
• Plan and execute communication plans & methods to ensure customer satisfaction and enable improvements to be implemented during the course of a study.
• Able to resolve conflicts, influence and communicate with key stakeholders and customers.
• Set up and test RBM system at study level to ensure system quality.
• Define key risk indicators (KRIs) in study system, and ensure consistency between the standard level and the study level.

Kenntnisse

Clinical data management

RBM understanding

Quality oversight

Ausbildung

Bachelor’s degree or above in scientific or business related discipline

Tools

Oracle

PL/SQL

SAS

Java

Jobbeschreibung

Pfizer in Buenos Aires offers a hybrid Senior Associate, Central Monitor role focused on RBM-enabled data surveillance in clinical studies. You will help ensure data integrity and regulatory compliance while supporting global study teams.

The position requires 3-5 years in clinical development, strong data management and technical skills, and the ability to coordinate with stakeholders 2–3 days weekly in-office.