Senior Central Monitor, RBM Data Surveillance

Chainlink Labs; Quilmes; Ibrido; ARS 138.361.000 - 184.482.000; Tempo pieno

Descrizione del lavoro

Pfizer is seeking a Senior Associate, Central Monitor to ensure data completeness, quality and integrity in the RBM‑driven clinical data framework. The role emphasizes risk-based monitoring, KRIs setup, and regulatory compliance across global studies.

Hybrid work location in Buenos Aires, Argentina with 2–3 office days per week. Responsibilities include implementing global RBM strategies, testing RBM systems at study level, reviewing outputs for signal and action management, and collaborating

Competenze

• Bachelor’s degree or above in a scientific or business discipline.
• 3–5 years experience in the clinical development fields.
• Experience in data management concepts (CRF design, database setup, edit checks, DMPs, data cleaning).
• Knowledge of clinical trial databases and their applications.
• Good knowledge of Windows environment (Word, Excel, PowerPoint, Project).
• Experience with Oracle, PL/SQL, SAS, Java and relational databases.
• Strong communication and project management skills; independent work ability.

Mansioni

• Implement global RBM strategies and standards to ensure quality outputs.
• Set up and test RBM systems at study level; define KRIs.
• Review study system outputs for signal and action management.
• Plan and execute communication plans to improve customer satisfaction.
• Coordinate with stakeholders and ensure regulatory/compliance alignment.
• Ensure quality oversight in central monitor activities.

Conoscenze

Clinical development knowledge

Study design understanding

Communication skills

Project management

Formazione

Bachelor’s degree or above in scientific or business discipline

Strumenti

Oracle

PL/SQL

SAS

Java

Relational databases

Descrizione del lavoro

Pfizer is seeking a Senior Associate, Central Monitor to ensure data completeness, quality and integrity in the RBM‑driven clinical data framework. The role emphasizes risk-based monitoring, KRIs setup, and regulatory compliance across global studies.

Hybrid work location in Buenos Aires, Argentina with 2–3 office days per week. Responsibilities include implementing global RBM strategies, testing RBM systems at study level, reviewing outputs for signal and action management, and collaborating