About the Role
The SDTL / Central Monitoring Manager works within the Risk Management – Central Monitoring Group and leads clinical study teams in the study-specific design and implementation of Analytical Risk-Based Monitoring (ARBM) for clinical trials (Phase I–IV).
In this role, you will be responsible for a broad range of activities including:
Risk identification and mitigation
Data analysis and interpretation
Leading cross-functional teams
Multi-level communication with study team members
Ongoing training on ARBM-related processes
Participation in innovation and process improvement initiatives
Deliverables
GRAD (Level 0) / BASE (Level 1)
Services rendered will:
Adhere to applicable Sponsor SOPs, work instructions, policies, and local regulatory requirements.
Support central study teams (includi...
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