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Veeda Clinical Research (Veeda CR), a reputed organization in the pharmaceutical and clinical research domain, is hiring Clinical Research Associates (CRA) for its Ahmedabad location. This opportunity is ideal for professionals with 1–3 years of clinical research experience, strong knowledge of ICH-GCP guidelines, and hands-on exposure to site monitoring and compliance activities.
With competitive compensation, structured learning, and exposure to regulated clinical trials, this Clinical Research Associate job at Veeda CR offers an excellent career pathway for aspiring CRAs in India.
Job Overview
- Position: Clinical Research Associate
- Company: Veeda Clinical Research (Veeda CR)
- Location: Ahmedabad, Gujarat
- Experience Required: 1–3 years
- Salary: ₹2.5 – ₹4.0 LPA (as per experience & skills)
- Employment Type: Full-time, Permanent
- Openings: 2
- Industry: Pharmaceutical & Life Sciences
Key Responsibilities of Clinical Research Associate
1. Off-Site Monitoring
- Conduct off-site monitoring visits across different phases of clinical studies
- Perform Initial Site Visits (ISV) to train and guide site personnel
- Verify protocol prerequisites and assess site readiness
- Execute routine monitoring visits as per study monitoring plan
2. Communication & Documentation
- Coordinate with potential sites for Feasibility Assessment Questionnaires (FAQ)
- Prepare and submit:
- Pre-Study Qualification Reports
- Site Initiation Visit (SIV) Reports
- Site Monitoring Visit (SMV) Reports
- Site Close-Out Visit (SCOV) Reports
- Collect essential documents such as calibration certificates, agreements, and approvals
- Ensure accurate data capture using logs, trackers, source data templates, and study forms
3. Audits & Regulatory Compliance
- Review study documents for compliance with SOPs, protocols, and regulatory guidelines
- Support audits and inspections by Sponsors, QA/QC, and Regulatory Authorities
- Train and mentor off-site teams on:
- ICH-GCP
- Root Cause Analysis (RCA)
- Updated regulatory requirements
- Perform additional responsibilities as assigned by the reporting manager
Eligibility & Qualifications
- Education:
- M.Pharm (Any Specialization)
- M.Sc / MS (Life Sciences or related discipline)
- Experience:
- 1–3 years of experience in clinical research or CRA roles
- Key Skills:
- ICH-GCP guidelines
- Site monitoring
- Clinical trial documentation
- Regulatory compliance
- Communication with investigators and sites
Why Join Veeda CR?
- Exposure to global clinical research projects
- Strong compliance-driven work culture
- Learning opportunities in audits, monitoring, and regulations
- Career growth in CRA and clinical operations roles
- Competitive salary aligned with industry standards
How to Apply?
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