-To ensure that all Quality Assurance related activities surrounding a clinical trial amp; the other RAY services are compliant with all regulatory requirements and CP standards
-Establishing a document Control system and ensure compliance of SOPs with the local regulations amp; ICH-GCP.
-Ensure that proper on the job Training Schedule is set to every employee in RAY
-Responsible for Conducting internal and external audits to ensure compliance with company SOPs, GCP and local regulations.
-Conduct audits of clinical Study documents, including Investigator Brochutres, Clinical Protocols, Clinical Study Reports, Case Report Forms and Informed Consent Form
Requirements