Clinical Data Management Jobs | Syngene is Hiring a CDM QA Auditor | Apply Now
Ready to elevate your career in clinical data management jobs with a global research organization? Syngene careers now offer an exciting opportunity for experienced professionals to step into a high-impact QA jobs role as a CDM QA Auditor. Based in Bengaluru, this position places you at the core of clinical quality, regulatory compliance, and data integrity across multi-phase clinical studies, ideal for life science professionals aiming to grow in clinical research quality assurance.
Job Details
- Job Title: CDM QA Auditor
- Location: Bengaluru, India
About the Company
Syngene is an innovation-led contract research, development, and manufacturing organization providing integrated scientific services from early discovery to commercial supply. The company supports global pharmaceutical and biotechnology clients through high-quality research solutions. Safety, quality, and integrity are embedded into all Syngene careers. With a strong compliance culture, Syngene enables impactful clinical data management jobs across global clinical development programs.
Key Responsibilities
- Perform QA audits for clinical data management activities across various phases of studies.
- Verify compliance with ICH-GCP (R2), study protocols, and regulatory requirements.
- Assist in the development and review of SOPs for clinical data management.
- Collate data for quality metrics and report trends in CDM related functions.
- Conduct vendor/sub-contractor audits and follow-ups.
- Collaborate with CDM operations for continuous improvement and compliance.
- Plan & conduct co-audits with compliance QA team.
- Follow-up on audit observations, ensuring timely resolutions.
- Maintain and update Syngene QA tools and systems.
- Facilitate sponsor audits and regulatory inspections.
- Recognize and propose process improvements.
- Conduct various GxP audits and report findings.
Skills Required
- Strong knowledge of clinical data management processes
- Expertise in GCP, CDISC, and regulatory compliance
- Experience in QA audits and inspection readiness
- Understanding of EDC platforms and CRF design
- Excellent documentation, reporting, and communication skills
- Ability to work independently in high-responsibility
This opportunity within Syngene careers is ideal for professionals seeking advanced clinical data management jobs with real regulatory impact. If you are passionate about quality, compliance, and clinical research excellence, this CDM QA Auditor role offers long-term growth, exposure to global audits, and a strong career path in QA jobs.
