Project role : Associate Site Report Specialist
Work experiences : 4 to 6 years.
Work location : Homebased
Must have skills : CRA, Clinical Research Associate, Onsite Monitoring
Job overview : Review Site Visit Reports (SVRs) to ensure they meet or exceed quality standards and support goals of quality, subject safety, data integrity and regulatory compliance. Use tools and techniques to ensure the efficient and effective review of Site Visit Reports and their associated attachments, in compliance with IQVIA SOP, ICH/ GCP guidelines, and protocol requirements.
Job Responsibility:

Keyskills: Clinical Research associate Site Monitoring CRA
IQVIA Biotech provides clinical development services to the pharmaceutical, biotech, and medical device industries. They specialize in supporting smaller biotech firms by offering expertise in clinical trials, regulatory compliance, and drug development.