$57,500.00 - $226,800.00; not specified; not speci...
Site monitoring visits
Subject recruitment plan
Protocol and study training
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the study protocol, regulations, and sponsor requirements
Job Summary
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the study protocol, regulations, and sponsor requirements.
Manage study progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution, potentially supporting the start-up phase.
Ensure site documents are available for filing in the Trial Master File and verify the Investigator's Site File is maintained according to GCP and local regulatory requirements.
Matching Summary
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the study protocol, regulations, and sponsor requirements.
Salary
$57,500.00 - $226,800.00; Not specified; Not specified
Skills & Requirements
Must-have
Site monitoring visits
Subject recruitment plan
Protocol and study training
Quality and integrity evaluation
Trial Master File maintenance
Site management documentation
Nice-to-have
Effective time management
Problem-solving skills
Client relationship management
Key Requirements
Minimum 2 years on-site monitoring experience
Bachelor's Degree in scientific discipline or healthcare preferred
Knowledge of GCP and ICH guidelines
Proficiency in Microsoft Word, Excel, PowerPoint
Written and verbal communication skills in English
Work Rights
Must reside in the country where the job is located