Clinical Research QA Job in Ahmedabad at Clinvigilant. Candidates with 3+ years experience in GCP and audits eligible.
Company Overview
Clinvigilant is a growing organization operating in the clinical research and pharmacovigilance domain, focused on maintaining high-quality standards in clinical trials and regulatory compliance. The company works closely with industry guidelines such as ICH-GCP and ensures robust quality systems across all processes.
With a commitment to accuracy, compliance, and continuous improvement, Clinvigilant provides professionals with an opportunity to work in a structured environment that emphasizes documentation quality, audit readiness, and regulatory excellence. Clinical Research QA Job in Ahmedabad at Clinvigilant
Job Overview (Job Details)
| Job Title | Quality Assurance (QA) Professional |
|---|---|
| Company | Clinvigilant |
| Location | Ahmedabad, Gujarat |
| Qualification | B.Pharm / M.Pharm / Life Sciences / Clinical Research |
| Experience | Minimum 3+ Years |
| Employment Type | Full-Time (On-site) |
| Department | Quality Assurance (Clinical Research) |
| Salary | ₹4.0 – ₹7.5 LPA (Estimated) |
Job Location & Employment Type
- Location: Ahmedabad, Gujarat, India
- Employment Type: Full-Time (On-site)
- Industry: Clinical Research / Pharmacovigilance / Quality Assurance
This role is best suited for professionals with prior experience in clinical QA who want to strengthen their expertise in regulatory compliance and audit systems. Clinical Research QA Job in Ahmedabad at Clinvigilant
Open Position / Department Details
- Position: Quality Assurance (QA) Professional
- Department: Clinical Quality Assurance
The selected candidate will play a key role in ensuring that clinical research processes meet regulatory and quality standards while supporting audits and compliance systems. Clinical Research QA Job in Ahmedabad at Clinvigilant
Key Roles & Responsibilities
Clinical Quality & Compliance
- Ensure adherence to ICH-GCP guidelines and internal SOPs
- Monitor clinical processes to maintain regulatory compliance
- Support implementation of quality systems across clinical research activities
Documentation & SOP Management
- Review, update, and approve Standard Operating Procedures (SOPs)
- Maintain accurate QA documentation, records, and databases
- Ensure document control and version management
Audit & Inspection Readiness
- Conduct internal audits and prepare detailed audit reports
- Identify compliance gaps and recommend improvements
- Maintain readiness for external audits and inspections
CAPA & Quality Improvement
- Identify deviations and implement Corrective and Preventive Actions (CAPA)
- Track CAPA effectiveness and ensure closure
- Promote continuous improvement in QA systems
Data Integrity & Regulatory Support
- Ensure data integrity across clinical processes
- Support regulatory inspections and compliance requirements
- Assist teams in maintaining quality standards during clinical trials
Clinical Research QA Job in Ahmedabad at Clinvigilant
Eligibility Criteria
Education
- B.Pharm / M.Pharm
- Life Sciences / Clinical Research or related discipline
Experience
- Minimum 3 years of experience in Quality Assurance within clinical research
- Experience in SOP handling, audits, and regulatory compliance is essential
Skills Required
- Strong knowledge of ICH-GCP guidelines
- Understanding of clinical trial processes and regulatory frameworks
- Experience in QA documentation and audit handling
- Good analytical and problem-solving skills
- Strong attention to detail and accuracy
- Effective communication and coordination abilities
Clinical Research QA Job in Ahmedabad at Clinvigilant
Salary & Benefits
- Estimated Salary: ₹4,00,000 – ₹7,50,000 per annum
- Performance-based growth opportunities
- Exposure to clinical research quality systems
- Opportunity to work on regulatory compliance and audits
- Professional development in QA and clinical research
Selection Process
The hiring process may include:
- Resume shortlisting
- HR discussion
- Technical interview focusing on QA, GCP, and audits
- Final selection
How to Apply
- Interested candidates can apply by sending their updated CV via email application (as mentioned in the original job post).
- Ensure your resume highlights QA experience, audit exposure, and regulatory knowledge.
Important Dates
- No last date mentioned – apply at the earliest
Why Apply for This Pharma Job?
This opportunity at Clinvigilant is ideal for professionals aiming to grow in clinical quality assurance and regulatory compliance. The role provides exposure to real-world clinical trial quality systems, SOP management, and audit processes.
Working in this position will enhance your understanding of global regulatory requirements such as ICH-GCP and help you build expertise in CAPA management and inspection readiness. It also opens doors to advanced roles in clinical QA, pharmacovigilance, and regulatory affairs.
Professionals seeking stability, career growth, and specialization in clinical research quality systems will find this role highly beneficial. Clinical Research QA Job in Ahmedabad at Clinvigilant
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with Clinvigilant or its recruitment process. Candidates are advised to verify all details from official sources before applying. We do not charge any fees for job postings or applications. Clinical Research QA Job in Ahmedabad at Clinvigilant
Final Call-to-Action
If you have experience in clinical quality assurance and want to advance your career in regulatory compliance and audits, this role is a strong opportunity. Apply now by sending your updated CV and take the next step toward a rewarding career in clinical research QA. Clinical Research QA Job in Ahmedabad at Clinvigilant
