QC Reviewer Role at Cliantha Research Limited | Grab your Opportunity Now!
Looking for a career in clinical research? The QC Reviewer (Clinic) role in Vadodara offers an exciting opportunity for B. Pharma, M. Pharma, or M.Sc. graduates with 2-4 years of QC experience. Contribute to high-quality clinical studies by reviewing raw data, ensuring compliance with GCP, SOPs, and regulatory guidelines, and supporting QA audits.
Job Description:
- Job Location: Vadodara, Gujarat
- Education: B. Pharma/M. Pharma, M.Sc.
- Experience: 2-4 years of QC experience in the clinical research industry.
About the Company:
Cliantha Research Limited is a leading clinical research organization dedicated to ensuring high-quality research outcomes and compliance with regulatory guidelines. Our team is committed to excellence in clinical data management and review.
Key Responsibilities for the QC Reviewer Role:
- Reviewing clinical raw data according to the predefined Quality Control Plan to ensure completeness, accuracy, and compliance with the Study Protocol, GCP, SOPs, and regulatory guidelines.
- Conducting online monitoring of study activities to ensure adherence to GCP, SOPs, Protocol, and applicable regulatory guidelines.
- Managing issuance, reconciliation, and accountability of controlled forms and documents per SOPs.
- Preparing projects for QA audits and proper archiving.
- Reviewing tabular listings attached to Clinical Study Reports and performing Individual Subject CRF scan checks as required.
- Assisting the QC in-charge in reviewing Quality Control-Clinic SOPs.
- Undertaking any additional responsibilities assigned by the Head of Department or Management.
- Performing source data verification (SDV) activities as required by the sponsor.
- Reviewing safety lab data in accordance with the Data Transfer Agreement.
Career Growth Opportunities in Clinical QC:
The QC Reviewer role offers significant career growth potential within the clinical research industry. Professionals in this position can progress to senior QC roles, QA oversight positions, or project management responsibilities. By gaining hands-on experience with data review, source data verification (SDV), and regulatory compliance, candidates enhance their expertise and open doors to leadership opportunities in clinical research organizations. Continuous learning and exposure to diverse studies ensure long-term professional development.
Why Join as a QC Reviewer (Clinic):
Joining in this QC Reviewer role allows you to contribute directly to high-quality clinical studies while ensuring patient safety and data integrity. This role provides an opportunity to work with experienced professionals, gain in-depth knowledge of GCP, SOPs, and regulatory guidelines, and participate in cutting-edge clinical research projects. Candidates benefit from a collaborative environment, structured processes, and the chance to make a meaningful impact on healthcare outcomes.
