Junior Auditor – Ahmedabad, India
Company: Veeda Clinical Research
Location: Ahmedabad, India
Employment Type: Full-Time, Permanent
Experience Required: 1–3 Years
Salary: ₹3–5 LPA
Openings: 2
Job Overview
Veeda Clinical Research is seeking a Junior Auditor to join our Quality Assurance (QA) team. The role is ideal for candidates with 1–3 years of experience in clinical trial auditing, BA/BE studies, or Phase I trials. The Junior Auditor will work under the supervision of senior QA personnel, supporting the planning, execution, and reporting of audits while ensuring compliance with GCP, SOPs, and regulatory standards.
This role offers exposure to clinical, statistical, vendor, and sponsor audits, making it suitable for B.Sc, B.Pharm, M.Sc, or M.Pharm graduates seeking a career in quality assurance and clinical compliance.
Key Responsibilities
Audit Planning & Execution
Assist in preparing audit plans for BA/BE and Phase I clinical studies in consultation with senior auditors
Conduct in-process and retrospective audits of clinical and statistical phases under guidance
Reporting & Documentation
Prepare and issue audit reports (in-process and retrospective) with senior QA review
Support compliance verification of audit responses and closure of audit findings
Review draft and final study reports for quality assurance
Issue QA authentication for study documents
Support in Specialized Audits
Assist senior auditors in system audits, vendor audits, and sponsor audits
Contribute to trend analysis and distribution of audit-related documents
Ensure proper documentation control and maintenance for QA compliance
Additional Responsibilities
Perform any other tasks assigned by the QA Auditor to support the audit and compliance process
Required Qualifications & Skills
Undergraduate Degree: B.Sc or B.Pharm in any specialization
Postgraduate Degree (preferred): M.Sc or M.Pharm in any specialization
1–3 years of experience in clinical trial auditing, quality assurance, or regulatory compliance
Knowledge of BA/BE studies, Phase I trials, in-process and retrospective audits
Strong attention to detail, analytical skills, and documentation proficiency
Understanding of GCP, SOPs, and clinical trial processes
Preferred Skills
Familiarity with clinical trial phases, statistical data audits, and vendor compliance audits
Ability to work under guidance, learn audit methodologies, and support senior QA personnel
Strong written and verbal communication skills
About Veeda Clinical Research
Veeda CR is a leading Contract Research Organization (CRO) offering end-to-end clinical trial services to pharmaceutical, biotechnology, and medical device companies. Our focus on quality, compliance, and regulatory excellence ensures reliable, high-standard clinical research outcomes.
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