CDM QA Auditor
Location: Bengaluru, Karnataka, India – 560100
Division: Essential Functions
Company: Syngene International Ltd.
Employment Type: Full-Time
Posted Date: 11 February 2026
About Syngene
Syngene International Ltd. is an innovation-led Contract Research, Development, and Manufacturing Organization (CRDMO) delivering integrated scientific services from early discovery to commercial supply. With a strong global client base, Syngene operates under stringent regulatory, quality, and data integrity standards aligned with international GxP frameworks.
Safety, compliance, and operational excellence are embedded into Syngene’s culture, with Environment, Health, and Safety (EHS) standards treated at par with business performance.
Role Overview
The CDM QA Auditor will be responsible for Quality Assurance oversight of Clinical Data Management (CDM) activities across BA/BE studies and Phase I–IV clinical trials. The role ensures compliance with ICH-GCP (R2), CDISC standards, study protocols, regulatory requirements, and internal SOPs.
This position requires expertise in GCP auditing, vendor qualification audits, regulatory inspection readiness, CAPA management, and quality system improvement within a clinical development environment.
Key Responsibilities
Clinical Data Management QA Oversight
Conduct QA audits and reviews of CDM activities for BA/BE and Phase I–IV clinical trials
Verify compliance with ICH-GCP (R2), Data Management Plans (DMP), study protocols, and regulatory requirements
Review CRFs, database annotations, and EDC configurations to ensure protocol alignment
Evaluate CDISC standards and study data compliance
Collate and analyze CDM quality metrics and identify trends
Audit Execution & Reporting
Plan, schedule, conduct, and report GxP audits independently or with minimal supervision
Perform vendor/sub-contractor qualification and surveillance audits (onsite or remote)
Lead or participate in co-audits with sponsor representatives or QA teams
Document audit findings and ensure corrective and preventive actions (CAPA) are implemented and closed within timelines
Review qualification and validation documentation of computerized systems, where applicable
Regulatory & Sponsor Audit Support
Facilitate sponsor audits and regulatory inspections related to clinical data management
Collaborate with CDM operations to resolve audit findings in accordance with GCP and best GxP practices
Support regulatory inspection readiness planning and execution
Quality Systems & Continuous Improvement
Maintain and update QA systems, records, and tools
Assist in development and review of QA and cross-functional SOPs
Identify opportunities for procedural and process improvements within CDM
Deliver GCP and QA training sessions to internal teams
Escalate vendor performance issues and support corrective action planning
Safety & Compliance Responsibilities
Ensure adherence to Syngene’s EHS, data integrity, and quality policies
Complete mandatory compliance training
Contribute to safety metrics governance and review
Required Qualifications
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Clinical Research, or related discipline
Minimum 5–8 years of experience in Clinical Data Management and/or GCP Quality Assurance auditing
Strong knowledge of ICH-GCP (R2), CDISC standards, and international regulatory frameworks
Experience conducting GxP audits, vendor audits, and sponsor audit support
Expertise in CAPA management and quality systems
Experience with EDC systems, database review, and computerized system validation documentation
Strong analytical, reporting, and communication skills
Willingness to travel nationally and internationally as required
Preferred Qualifications
Experience within a CRO or clinical development organization
Exposure to BA/BE studies and patient-based Phase I–IV clinical trials
Demonstrated leadership in co-audits and regulatory inspections
Advanced understanding of global regulatory inspection requirements
Why Consider This Opportunity
This role offers an opportunity to lead GCP quality assurance initiatives within a globally recognized CRDMO. As a CDM QA Auditor, you will play a strategic role in ensuring clinical data integrity, regulatory compliance, and audit excellence across global clinical development programs.
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