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Veeda Clinical Research is inviting applications for the position of Clinical Research Associate (CRA) at its Ahmedabad location. This opportunity is ideal for clinical research professionals with 1–3 years of experience in ICH-GCP–compliant clinical trials and strong exposure to off-site monitoring and site management.
Veeda CR is a well-established CRO in India, supporting global and domestic clinical trials across multiple therapeutic areas. This role offers hands-on involvement across the entire clinical trial lifecycle, making it a strong career-building opportunity for aspiring CRAs.
🔍 Job Overview
- Job Title: Clinical Research Associate
- Company: Veeda Clinical Research (Veeda CR)
- Location: Ahmedabad, Gujarat
- Experience Required: 1 – 3 Years
- Salary: ₹2.5 – 4.0 LPA
- Job Type: Full-Time
- Openings: 2
- Posted On: Today
🧩 Key Responsibilities
1. Off-Site Monitoring
- Conduct off-site monitoring visits during various study phases
- Perform Site Initiation Visits (SIVs) and ensure study readiness
- Review protocol prerequisites and site compliance
- Execute routine monitoring as per study monitoring plans
2. Communication & Documentation
- Coordinate with sites for feasibility assessments
- Prepare and submit:
- Pre-Study Qualification Reports
- Site Initiation Visit Reports
- Site Monitoring Visit Reports
- Site Close-Out Visit Reports
- Collect essential documents such as calibration certificates, agreements, and logs
- Support off-site teams with CRFs, source documents, trackers, and templates
3. Audits & Regulatory Compliance
- Review trial documents for SOP, protocol, and regulatory compliance
- Train and mentor off-site teams on ICH-GCP and regulatory updates
- Support internal QA audits and external sponsor/regulatory inspections
- Perform additional responsibilities as assigned by management
🎓 Qualifications & Skills Required
- Degree in Life Sciences / Pharmacy / Clinical Research
- 1–3 years of experience as a Clinical Research Associate or equivalent role
- Strong knowledge of ICH-GCP guidelines
- Experience in clinical trial monitoring and CRO operations
- Excellent documentation, communication, and coordination skills
💼 Why Join Veeda CR?
- Work with a reputed Indian CRO
- Exposure to global clinical trials
- Structured learning and mentoring environment
- Competitive salary aligned with industry standards
- Long-term growth in clinical research careers
📝 How to Apply
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