This role involves performing centralized monitoring activities to evaluate the quality and integrity of clinical studies according to protocols and regulations
Job Summary
This role involves performing centralized monitoring activities to evaluate the quality and integrity of clinical studies according to protocols and regulations.
The position requires managing study triggers, preparing i-site packs, and potentially conducting subject-level data reviews to ensure patient information accuracy.
Candidates must possess advanced English skills and be prepared to support clinical sites in either Latin America or North America from a home-based location.
Matching Summary
This role involves performing centralized monitoring activities to evaluate the quality and integrity of clinical studies according to protocols and regulations.
Skills & Requirements
Must-have
Advanced Excel proficiency required
Remote monitoring experience mandatory
Review structured clinical data output
Manage triggers and i-site packs
Perform subject level data review
Nice-to-have
Experience with trend analytics
Cross-functional team collaboration
Ability to triage new data issues
Strong communication skills for sites
Key Requirements
Bachelor's degree in life sciences or nursing qualification
Minimum 2 years of on-site or remote monitoring experience