Central Monitor Lead, RBM Data & Quality

Atomic Hr; Buenos Aires; Híbrido; ARS 700 000 - 1 100 000; Tempo integral

Resumo da oferta

Pfizer in Buenos Aires, Argentina, offers a hybrid role as Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences. The position emphasizes RBM-driven data quality and regulatory compliance, with 2–3 days per week in-office collaboration.

You will work with global study teams to define KRIs, monitor data integrity, and ensure study data quality across platforms, aligning with ICH GCP and SOPs.

Qualificações

• Bachelor’s degree or above of equivalent experience in a scientific or business related discipline.
• 3–5 years of experience in the clinical development field.
• Knowledge of the clinical development process and study design (Phase I–IV).
• Experience in data management: CRF design, database setup, edit checks, DMPs, and data cleaning.
• Knowledge of clinical trial databases and applications.
• Familiarity with Windows tools (Word, Excel, PowerPoint, Project).
• Experience with Oracle, PL/SQL, SAS, Java and relational databases.
• Strong project management, independent work, and communication skills.

Responsabilidades

• Implement global RBM strategies, processes, and standards to ensure quality and timely delivery.
• Set up and test study-level RBM systems and KRIs.
• Review study outputs for signal and action management.
• Plan communications to ensure customer satisfaction and drive improvements.
• Coordinate with stakeholders and resolve conflicts effectively.
• Ensure quality oversight in central monitoring activities.
• Maintain documentation for RBM activities and data integrity.

Conhecimentos

Project management

Verbal and written communication

Time management

Independent work

Formação académica

Bachelor’s degree or above in science or related field

Ferramentas

Oracle

PL/SQL

SAS

Java

Descrição da oferta de emprego

Pfizer in Buenos Aires, Argentina, offers a hybrid role as Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences. The position emphasizes RBM-driven data quality and regulatory compliance, with 2–3 days per week in-office collaboration.

You will work with global study teams to define KRIs, monitor data integrity, and ensure study data quality across platforms, aligning with ICH GCP and SOPs.