senior Central Monitor, Data Surveillance, Clinical Data Sciences
Data Science Jobs
Chennai, India
Hybrid
Risk-based monitoring system development
Clinical trial database management
Key risk indicators (kris) definition
The Senior Central Monitor at Data Science Jobs in Chennai, India, is responsible for ensuring the quality and integrity of clinical trial data under a Risk-Based Monitoring (RBM) approach. The role requires extensive experience in clinical development, data management, and technical expertise in various data systems
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 mode.
The role involves developing and implementing Risk-Based Monitoring systems, defining key risk indicators, and managing data review and issue resolution in compliance with regulations and SOPs.
The Senior Central Monitor works with global study teams to meet study objectives and ensures quality oversight and control steps are implemented in central monitoring activities.
Matching Summary
Match Score: 85
The Senior Central Monitor at Data Science Jobs in Chennai, India, is responsible for ensuring the quality and integrity of clinical trial data under a Risk-Based Monitoring (RBM) approach. The role requires extensive experience in clinical development, data management, and technical expertise in various data systems.
Skills & Requirements
Must-have
Risk-Based Monitoring system development
Clinical trial database management
Key risk indicators (KRIs) definition
Data quality assessment setup
Oracle, PL/SQL, SAS, Java skills
Clinical data review and signal management
Regulatory compliance and SOP adherence
Nice-to-have
Project management skills
Effective verbal and written communication
Conflict resolution and stakeholder influence
Cross-study learning documentation
Hybrid work environment
Windows Office applications proficiency
Independent working ability
Key Requirements
Bachelor’s degree or equivalent experience
Minimum 7 years clinical development experience
Knowledge of clinical development phases I-IV
Experience in data management and clinical trial databases
Technical expertise in Oracle, PL/SQL, SAS, Java
Understanding of ICH GCP and regulatory requirements