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Cdm Qa Auditor

Syngene
Syngene
5-8 years
Not Disclosed
Bengaluru, Karnataka, India
10 Feb. 12, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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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