Posted:11 hours ago|
Platform:
On-site
Full Time
Company Description Cliantha Research Limited is a full-service Clinical Research Organization (CRO) offering comprehensive services in various research areas. The company provides ethical, customer-centric services to pharmaceutical, biotech, and healthcare companies globally. With a strong team of professionals and advanced facilities in multiple countries, Cliantha is a leader in the field of clinical research. Role Description This is a full-time on-site role for a QC Reviewer at Cliantha Research Limited. The QC Reviewer will be responsible for conducting quality control reviews of clinical research data and documentation. Review of clinical raw data as per predefined Quality Control Plan for completeness, accuracy, and for compliance with the Study Protocol, GCP, SOPs and applicable regulatory Guidelines. Online Monitoring of study activities to ensure that studies are conducted in accordance with GCP, SOPs, Protocol and applicable regulatory guidelines. Job Location: Vadodara (On-site) Qualifications 2-4 years of experience in Quality Control reviews and data analysis Knowledge of regulatory requirements in clinical research Excellent communication and documentation skills Bachelor's degree in a relevant field (Life Sciences, Pharmacy, etc.) Show more Show less
Cliantha Research Limited
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My Connections Cliantha Research Limited
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