Senior Associate, ​​senior Central Monitor, Data Surveillance, Clinical Data Sciences​

pfizer.ch

Hybrid
Risk based monitoring system development
Key risk indicators (kris) definition
Data quality assessment
The Senior Central Monitor is responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode

Job Summary

  • The Senior Central Monitor is responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode.
  • Develop, implement and maintain Quality Control related documentations for RBM related activities to ensure data completeness and accuracy.
  • Works with the global study team to meet the study objectives and ensures risk based monitoring activities comply with regulations, applicable Standard Operating Procedures (SOPs) and Processes at all times.

Matching Summary

The Senior Central Monitor is responsible for ensuring the completeness, quality and integrity of the subject data in the clinical trial database under Risk Based Monitoring (RBM) mode.

Skills & Requirements

Must-have

  • Risk Based Monitoring system development
  • Key Risk Indicators (KRIs) definition
  • Data quality assessment
  • ICH GCP compliance
  • Clinical trial database management

Nice-to-have

  • Global study team collaboration
  • Customer satisfaction focus
  • Cross-study learning documentation

Key Requirements

  • Bachelor’s degree or equivalent experience
  • Minimum 7 years of relevant working experience
  • Experience in Oracle, PL/SQL, SAS, Java
  • Knowledge of clinical development process
  • Experience in data management role

Work Rights

Not specified

Tailored Resume

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