Website Cliantha Research
About Cliantha Research
Cliantha Research is a full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With the motto “Science with Integrity”, Cliantha has built a strong reputation backed by 15 years of flawless regulatory history with global agencies including USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
Position Details
Job Title: Clinical Trials QA Auditor
Department: Quality Assurance (QA)
Location: Cliantha Corporate, Ahmedabad
Qualifications
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M.Sc., B.Pharm, M.Pharm, or equivalent qualification
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8–12 years of relevant experience in QA within the clinical research/pharma industry
Key Skills & Expertise
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Strong knowledge of Quality Management Systems (QMS)
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Expertise in auditing and inspection readiness
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Experience in computer system validation (CSV), qualification, and compliance
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Proven ability in sponsor handling and stakeholder communication
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In-depth understanding of global regulatory guidelines and compliance requirements
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Strong time management and organizational skills
Key Responsibilities
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Conduct internal and external audits to ensure regulatory compliance and adherence to QMS
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Support inspection readiness activities for regulatory authorities
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Oversee CSV validation and qualification processes
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Collaborate with sponsors and stakeholders to ensure project quality and compliance
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Ensure timely completion of audit activities and documentation
Why Join Cliantha Research?
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Work with a global CRO recognized for integrity and regulatory excellence
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Opportunity to engage with international regulatory standards and high-profile projects
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Collaborative and ethical work culture with strong professional growth prospects
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To apply for this job please visit www.cliantha.com.