Perform monitoring and site management work to ensure sites are conducting studies and reporting data as required by protocol, regulations, and sponsor requirements
Job Summary
Perform monitoring and site management work to ensure sites are conducting studies and reporting data as required by protocol, regulations, and sponsor requirements.
Evaluate the quality and integrity of study site practices related to protocol conduct and adherence to regulations, escalating issues as appropriate.
IQVIA provides advanced analytics, technology solutions, and contract research services to the life sciences industry, enabled by its global workforce.
Matching Summary
Perform monitoring and site management work to ensure sites are conducting studies and reporting data as required by protocol, regulations, and sponsor requirements.
Skills & Requirements
Must-have
Perform site monitoring visits
Evaluate study site quality and integrity
Manage study progress and documentation
Ensure GCP and regulatory adherence
Subject recruitment plan management
Nice-to-have
Pushing boundaries of human science
Data science for impact
Intellectual curiosity and courage
Key Requirements
At least 2 years of on-site monitoring experience
Bachelor's Degree in scientific discipline or health care preferred
Good Clinical Practice (GCP) and ICH guidelines knowledge
Proficiency in Microsoft Word, Excel, and PowerPoint
Written and verbal communication skills in English