India’s clinical research sector is expanding fast, and with it comes a strong demand for Quality Assurance (QA) professionals who can safeguard patient safety, data integrity, and regulatory compliance. If you have hands-on experience with clinical trials, audits, SOPs, CAPA, and inspection readiness, this full-time onsite opportunity in Navi Mumbai could be your next career move.
A reputed Clinical Research Organization (CRO), Clinexel CRO, is hiring for multiple Quality Assurance (Clinical Trials) roles—ideal for both experienced managers and early-career executives eager to grow in clinical research quality systems.
🔍 Open Positions
1️⃣ Quality Assurance (Clinical Trials) – Manager / Assistant Manager
This role suits seasoned QA professionals who can independently manage quality systems and lead site audits.
Key Responsibilities
- Conduct and manage clinical trial site audits
- Ensure compliance with ICH-GCP, SOPs, and regulatory guidelines
- Oversee CAPA, risk assessments, and follow-ups
- Support inspection readiness and regulatory submissions
- Review quality documentation and audit reports
- Collaborate with internal teams and external stakeholders
- Drive continuous quality improvement initiatives
Key Requirements
- Strong understanding of clinical trial processes
- Hands-on experience with SOPs, audits, and CAPA
- Solid knowledge of regulatory compliance and inspections
- Excellent documentation and reporting skills
- Strong risk assessment, problem-solving, and communication skills
Experience
- 3–4 years of relevant QA experience in clinical trials
2️⃣ QA Executive – Clinical Trials
Perfect for early-career professionals looking to build depth in QA operations and systems.
Key Responsibilities
- Support QA activities across clinical trial processes
- Assist in audits, SOP implementation, and compliance checks
- Maintain quality documentation and records
- Track and follow up on CAPA
- Participate in inspection preparation
- Assist with system implementation and user support
- Manage IT processes and user access controls
Key Requirements
- Understanding of clinical trial workflows
- Familiarity with SOPs, audits, and CAPA
- Knowledge of regulatory compliance and inspection readiness
- Strong documentation and organizational skills
- Good communication and coordination abilities
- Exposure to system support, troubleshooting, and user access management (plus)
Experience
- 1–2 years in QA or clinical research systems
📍 Job Location & Work Mode
- Location: Navi Mumbai
- Employment Type: Full-Time
- Work Mode: Onsite only (no remote/hybrid)
Candidates should be comfortable collaborating closely with cross-functional teams from the office.
💡 Why Build a QA Career in Clinical Trials?
- 📈 Long-term growth in the CRO & pharma ecosystem
- 🌍 Exposure to global regulatory standards
- 🔍 Direct involvement in audits and inspections
- 📄 Strong skill development in documentation & compliance
- 🤝 Regular interaction with sponsors, sites, and regulators
Whether you’re leading audits or strengthening QA systems as an executive, these roles offer meaningful, hands-on industry exposure.
📨 How to Apply
Send your updated CV to:
📧 careers@clinexel-cro.com
Feel free to share this opportunity with colleagues who might be a great fit.
🌟 Final Note
If you’re passionate about quality systems, audits, and clinical trial compliance, these QA roles in Navi Mumbai provide a solid platform to advance your career. With full-time stability, regulatory exposure, and real responsibility, this is an opportunity worth grabbing.
Apply today and take the next step in your Clinical Trials QA career
