Cliantha is seeking a skilled QC Reviewer with clinic experience to join their team in Vadodara. This role involves reviewing clinical raw data for completeness, accuracy, and compliance with regulatory guidelines.
🧪About the Role
As a QC Reviewer, you will play a critical role in ensuring the quality of clinical data. Your primary responsibilities will include:
Clinical Data Review: Reviewing clinical raw data for completeness, accuracy, and compliance with the Study Protocol, GCP, SOPs, and applicable regulatory guidelines.
Quality Control: Ensuring that clinical data meets the predefined quality control plan and regulatory requirements.
Collaboration: Working with cross-functional teams to identify and resolve data quality issues.
🎓Requirements
Qualification: B. Pharma/M. Pharma, (link unavailable) or equivalent degree.
Experience: 2-4 years of QC experience in the clinical research industry.
Skills:
Strong understanding of GCP, SOPs, and regulatory guidelines.
Excellent analytical and problem-solving skills.
Ability to work independently and prioritise tasks effectively.
💼What We Offer
Career Growth: Opportunities for professional development and growth in a leading clinical research organisation.
Collaborative Environment: A dynamic and supportive team environment.
Competitive Benefits: Competitive salary and benefits package.
🌍Why Choose Cliantha?
Industry Leader: Opportunity to work with a leading clinical research organisation.
Professional Development: Opportunities for professional growth and development.
Innovative Culture: A company that values innovation and quality.
📧 Interested candidates can send their CV to recruitment1@cliantha.com